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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 10-Q
(Mark One)
x | QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 |
For the quarterly period ended June 30, 2010
OR
¨ | TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 |
Commission File Number 000-52045
Volcano Corporation
(Exact name of registrant as specified in its charter)
Delaware | 33-0928885 | |
(State or other jurisdiction of incorporation or organization) | (I.R.S. Employer Identification Number) | |
3661 Valley Centre Drive, Suite 200 San Diego, CA | 92130 | |
(Address of principal executive offices) | (Zip Code) |
(800) 228-4728
(Registrant’s telephone number, including area code)
Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes x No ¨
Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files). Yes ¨ No ¨
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company. See the definitions of “large accelerated filer,” “accelerated filer” and “smaller reporting company” in Rule 12b-2 of the Exchange Act. (Check one):
Large accelerated filer | ¨ | Accelerated filer | x | |||
Non-accelerated filer | ¨ (Do not check if a smaller reporting company) | Smaller reporting company | ¨ |
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes ¨ No x
Indicate the number of shares of each of the issuer’s classes of common stock, as of the latest practicable date:
Class | Outstanding at July 30, 2010 | |
Common stock, $0.001 par value | 50,663,682 |
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VOLCANO CORPORATION
Quarterly Report on Form 10-Q for the quarter ended June 30, 2010
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Item 1. | Financial Statements |
CONSOLIDATED BALANCE SHEETS
(in thousands, except per share data)
(unaudited)
June 30, 2010 | December 31, 2009 | |||||||
Assets | ||||||||
Current assets: | ||||||||
Cash and cash equivalents | $ | 50,628 | $ | 56,055 | ||||
Short-term available-for-sale investments | 76,970 | 66,028 | ||||||
Accounts receivable, net | 52,015 | 51,171 | ||||||
Inventories | 39,245 | 37,710 | ||||||
Prepaid expenses and other current assets | 4,717 | 5,892 | ||||||
Total current assets | 223,575 | 216,856 | ||||||
Restricted cash | 575 | 554 | ||||||
Long-term available-for-sale investments | 3,788 | — | ||||||
Property and equipment, net of accumulated depreciation of $39,267 and $32,539, respectively | 45,376 | 44,734 | ||||||
Intangible assets, net | 12,560 | 11,623 | ||||||
Goodwill | 931 | 931 | ||||||
Other non-current assets | 2,038 | 2,036 | ||||||
Total assets | $ | 288,843 | $ | 276,734 | ||||
Liabilities and Stockholders’ Equity | ||||||||
Current liabilities: | ||||||||
Accounts payable | $ | 12,508 | $ | 13,840 | ||||
Accrued compensation | 13,088 | 14,142 | ||||||
Accrued expenses and other current liabilities | 12,217 | 25,275 | ||||||
Deferred revenues | 5,047 | 4,881 | ||||||
Current maturities of long-term debt | 50 | 50 | ||||||
Total current liabilities | 42,910 | 58,188 | ||||||
Long-term debt | 85 | 110 | ||||||
Deferred revenues | 2,561 | 2,376 | ||||||
Other | 1,431 | 1,245 | ||||||
Total liabilities | 46,987 | 61,919 | ||||||
Commitments and contingencies(Note 4) | ||||||||
Stockholders’ equity: | ||||||||
Preferred stock, par value of $0.001; 10,000 shares authorized; no shares issued and outstanding at June 30, 2010 and December 31, 2009 | — | — | ||||||
Common stock, par value of $0.001; 250,000 shares authorized at June 30, 2010 and December 31, 2009; 50,660 and 48,790 shares issued and outstanding at June 30, 2010 and December 31, 2009, respectively | 51 | 49 | ||||||
Additional paid-in capital | 377,211 | 352,102 | ||||||
Accumulated other comprehensive loss | (3,529 | ) | (4,079 | ) | ||||
Accumulated deficit | (131,877 | ) | (133,257 | ) | ||||
Total stockholders’ equity | 241,856 | 214,815 | ||||||
Total liabilities and stockholders’ equity | $ | 288,843 | $ | 276,734 | ||||
See notes to unaudited consolidated financial statements.
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CONSOLIDATED STATEMENTS OF OPERATIONS
(in thousands, except per share data)
(unaudited)
Three Months Ended June 30, | Six Months Ended June 30, | |||||||||||||||
2010 | 2009 | 2010 | 2009 | |||||||||||||
Revenues | $ | 73,452 | $ | 54,042 | $ | 140,024 | $ | 103,001 | ||||||||
Cost of revenues, excluding amortization of intangibles | 27,093 | 22,486 | 53,731 | 43,135 | ||||||||||||
Gross profit | 46,359 | 31,556 | 86,293 | 59,866 | ||||||||||||
Operating expenses: | ||||||||||||||||
Selling, general and administrative | 30,082 | 26,453 | 63,161 | 51,533 | ||||||||||||
Research and development | 9,594 | 9,866 | 19,452 | 18,635 | ||||||||||||
Amortization of intangibles | 621 | 1,053 | 1,194 | 2,105 | ||||||||||||
In-process research and development | 33 | — | 65 | — | ||||||||||||
Total operating expenses | 40,330 | 37,372 | 83,872 | 72,273 | ||||||||||||
Operating income (loss) | 6,029 | (5,816 | ) | 2,421 | (12,407 | ) | ||||||||||
Interest income | 83 | 197 | 168 | 498 | ||||||||||||
Interest expense | (11 | ) | (1 | ) | (18 | ) | (3 | ) | ||||||||
Exchange rate (loss) gain | (423 | ) | 871 | (544 | ) | (257 | ) | |||||||||
Other, net | (9 | ) | — | (19 | ) | — | ||||||||||
Income (loss) before provision for income taxes | 5,669 | (4,749 | ) | 2,008 | (12,169 | ) | ||||||||||
Provision for income taxes | 253 | 518 | 628 | 712 | ||||||||||||
Net income (loss) | $ | 5,416 | $ | (5,267 | ) | $ | 1,380 | $ | (12,881 | ) | ||||||
Net income (loss) income per share: | ||||||||||||||||
Basic | $ | 0.11 | $ | (0.11 | ) | $ | 0.03 | $ | (0.27 | ) | ||||||
Diluted | $ | 0.10 | $ | (0.11 | ) | $ | 0.03 | $ | (0.27 | ) | ||||||
Shares used in calculating net income (loss) per share: | ||||||||||||||||
Basic | 50,452 | 48,335 | 50,099 | 48,184 | ||||||||||||
Diluted | 53,071 | 48,335 | 52,876 | 48,184 | ||||||||||||
See notes to unaudited consolidated financial statements.
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CONSOLIDATED STATEMENT OF STOCKHOLDERS’ EQUITY
(in thousands)
(unaudited)
Common Stock | Additional Paid-In Capital | Accumulated Deficit | Accumulated Other Comprehensive Loss | Total Stockholders’ Equity | ||||||||||||||||
Shares | Amount | |||||||||||||||||||
Balance at December 31, 2009 | 48,790 | $ | 49 | $ | 352,102 | $ | (133,257 | ) | $ | (4,079 | ) | $ | 214,815 | |||||||
Issuance of common stock under equity plans | 1,261 | 1 | 8,299 | 8,300 | ||||||||||||||||
Employee stock-based compensation cost | 5,841 | 5,841 | ||||||||||||||||||
Non-employee stock-based compensation cost | 325 | 325 | ||||||||||||||||||
Issuance of common stock related to acquisitions | 609 | 1 | 10,468 | 10,469 | ||||||||||||||||
Tax benefit related to stock-based compensation | 176 | 176 | ||||||||||||||||||
Comprehensive income | ||||||||||||||||||||
Net income | 1,380 | 1,380 | ||||||||||||||||||
Foreign currency translation adjustments | 558 | 558 | ||||||||||||||||||
Changes in net unrealized loss on available-for-sale investments | (8 | ) | (8 | ) | ||||||||||||||||
Total comprehensive income | 1,930 | |||||||||||||||||||
Balance at June 30, 2010 | 50,660 | $ | 51 | $ | 377,211 | $ | (131,877 | ) | $ | (3,529 | ) | $ | 241,856 | |||||||
See notes to unaudited consolidated financial statements.
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CONSOLIDATED STATEMENTS OF CASH FLOWS
(in thousands)
(unaudited)
Six Months Ended June 30, | ||||||||
2010 | 2009 | |||||||
Operating activities | ||||||||
Net income (loss) | $ | 1,380 | $ | (12,881 | ) | |||
Adjustments to reconcile net income (loss) to net cash provided by operating activities: | ||||||||
In-process research and development | 65 | — | ||||||
Depreciation and amortization | 8,819 | 7,018 | ||||||
Amortization of investment premium, net | 435 | 139 | ||||||
Non-cash stock-based compensation expense | 6,191 | 5,565 | ||||||
Other non-cash adjustments | (565 | ) | 257 | |||||
Loss on disposal of long-lived assets | 29 | 182 | ||||||
Changes in operating assets and liabilities: | ||||||||
Accounts receivable | (1,705 | ) | 5,362 | |||||
Inventories | (1,491 | ) | (4,855 | ) | ||||
Prepaid expenses and other assets | 517 | 1,560 | ||||||
Accounts payable | (586 | ) | 4,490 | |||||
Accrued compensation | (907 | ) | (1,063 | ) | ||||
Accrued expenses and other liabilities | (2,130 | ) | (1,882 | ) | ||||
Deferred revenues | 439 | (762 | ) | |||||
Net cash provided by operating activities | 10,491 | 3,130 | ||||||
Investing activities | ||||||||
Purchase of available-for-sale investments | (48,665 | ) | (85,355 | ) | ||||
Sale or maturity of available-for-sale investments | 33,856 | 47,911 | ||||||
Capital expenditures | (8,345 | ) | (12,312 | ) | ||||
Cash paid related to acquisitions | (596 | ) | (613 | ) | ||||
Cash paid for intangible assets | (2,149 | ) | (206 | ) | ||||
Proceeds from foreign currency exchange contracts | 1,417 | — | ||||||
Payment for foreign currency exchange contracts | (1,083 | ) | — | |||||
Net cash used in investing activities | (25,565 | ) | (50,575 | ) | ||||
Financing activities | ||||||||
Repayment of short-term debt | (1 | ) | (151 | ) | ||||
Repayment of long-term debt | (23 | ) | (28 | ) | ||||
Proceeds from sale of common stock under employee stock purchase plan | 1,234 | 998 | ||||||
Proceeds from exercise of common stock options | 7,067 | 791 | ||||||
Tax benefit related to stock-based compensation | 176 | — | ||||||
Repurchases of common stock | — | (416 | ) | |||||
Increases of restricted cash | (79 | ) | — | |||||
Release of restricted cash | — | 32 | ||||||
Net cash provided by financing activities | 8,374 | 1,226 | ||||||
Effect of exchange rate changes on cash and cash equivalents | 1,273 | (433 | ) | |||||
Net decrease in cash and cash equivalents | (5,427 | ) | (46,652 | ) | ||||
Cash and cash equivalents, beginning of period | 56,055 | 100,949 | ||||||
Cash and cash equivalents, end of period | $ | 50,628 | $ | 54,297 | ||||
Supplemental disclosures of cash flow information: | ||||||||
Cash paid for interest | $ | 18 | $ | 3 | ||||
Cash paid for income taxes | $ | 143 | $ | 1,202 | ||||
Supplemental disclosure of non-cash investing activities: | ||||||||
Issuance of common stock related to milestone payment | $ | 10,468 | $ | — |
See notes to unaudited consolidated financial statements.
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NOTES TO UNAUDITED CONSOLIDATED FINANCIAL STATEMENTS
June 30, 2010
(Unaudited)
1. Summary of Significant Accounting Policies
Basis of Presentation and Nature of Operations
The unaudited consolidated financial statements of Volcano Corporation (“we”, “us”, “our”, “Volcano” or the “Company”) contained in this quarterly report on Form 10-Q include our financial statements and the financial statements of our wholly-owned subsidiaries: Volcano Japan Co. Ltd. (“Volcano Japan”), Volcano Europe S.A./N.V. (“Volcano Europe”), Axsun Technologies, Inc. (“Axsun”) and Volcano Therapeutics South Africa (Pty) Ltd. (“Volcano South Africa”), a wholly-owned subsidiary of Volcano Europe. We design, develop, manufacture and commercialize a broad suite of intravascular ultrasound (“IVUS”) and functional measurement (“FM”) products that we believe enhance the diagnosis and treatment of vascular and structural heart disease. Our products consist of consoles which have been designed to serve as a multi-modality platform for our phased array and rotational IVUS catheters, fractional flow reserve (“FFR”) pressure wires and Medtronic’s Pioneer reentry device. We are developing additional offerings for integration into the platform, including forward-looking IVUS (“FL.IVUS”) catheters, image-guided therapy catheters and ultra-high resolution Optical Coherence Tomography (“OCT”) systems and catheters. Our IVUS products include single-procedure disposable phased array and rotational IVUS imaging catheters and additional functionality options such as virtual histology IVUS tissue characterization and ChromaFlo stent apposition analysis. Our FM offerings include FM consoles and single-procedure disposable pressure and flow guide wires used to measure the pressure and flow characteristics of blood around plaque, enabling physicians to gauge the plaque’s physiological impact on blood flow and pressure. We also develop and manufacture optical monitors, lasers, and optical engines used in OCT imaging systems as well as micro-optical spectrometers and optical channel monitors used in telecommunications and other industrial companies.
We have prepared the accompanying financial information at June 30, 2010 and for the three and six months ended June 30, 2010 and 2009, without audit, pursuant to the rules and regulations of the Securities and Exchange Commission (“SEC”). Certain information and footnote disclosures normally included in financial statements prepared in accordance with U.S. generally accepted accounting principles have been condensed or omitted pursuant to such rules and regulations. These unaudited consolidated financial statements should be read in conjunction with the audited consolidated financial statements and the notes thereto included in our annual report on Form 10-K for the year ended December 31, 2009.
In the opinion of management, the unaudited financial information at June 30, 2010 and for the three and six months ended June 30, 2010 and 2009 reflects all adjustments, which are normal recurring adjustments, necessary to present a fair statement of our financial position, results of operations and cash flows. The results of operations for the three and six months ended June 30, 2010 are not necessarily indicative of the operating results for the full fiscal year or any future periods.
Concentrations of Credit Risk
Goodman Company, Ltd. (“Goodman”) accounted for approximately 11% of our revenues for the six months ended June 30, 2009. No single customer accounted for more than 10% of our revenues for any other period presented, and at June 30, 2010 and December 31, 2009, no single customer accounted for more than 10% of our trade receivables.
On July 8, 2009, we entered into a Distributor Termination Agreement with Goodman that terminated certain agreements between us and Goodman effective August 31, 2009 and provided for the transition of the distribution, formerly handled by Goodman, of Volcano products in Japan to Volcano Japan.
We currently hold foreign exchange forward contracts with a single counterparty. The bank counterparty in these contracts exposes us to credit-related losses in the event of their non-performance and we do not require collateral for their performance. However, to mitigate that risk, we only contract with counterparties who meet our minimum credit quality guidelines. In addition, our exposure in the event of a default by our counterparty is limited to the changes in value of our hedged balances.
Stock-Based Compensation
We account for stock-based compensation under the provisions of the Financial Accounting Standards Board (“FASB”) Accounting Standards Codification (“ASC”) Topic 718,Compensation—Stock Compensation,(“ASC 718”), which requires the measurement and recognition of compensation expense for all stock-based awards made to employees and directors based on estimated fair values on the grant date. We recognize compensation expense for awards of equity instruments to employees and non-employees based on the grant-date fair value of those awards. See Note 5 “Stockholders’ Equity” for additional information.
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VOLCANO CORPORATION
NOTES TO UNAUDITED CONSOLIDATED FINANCIAL STATEMENTS—(Continued)
June 30, 2010
(Unaudited)
Net Income (Loss) Per Share
Basic and diluted net income (loss) per share is presented in accordance with FASB ASC Topic 260,Earnings per Share. Basic net income or loss per share is computed by dividing consolidated net income or loss by the weighted-average number of common shares outstanding during the period. Diluted net income or loss per share is computed by dividing consolidated net income or loss by the weighted-average number of common shares outstanding and dilutive potential common shares during the period. Our potentially dilutive shares include outstanding common stock options and restricted stock units. Such potentially dilutive shares are excluded when the effect would reduce net loss per share or increase net income per share. For the three months ended June 30, 2010 and 2009, and six months ended June 30, 2010 and 2009, potentially dilutive shares totaling 2.7 million, 4.4 million, 2.8 million, and 4.2 million, respectively, have not been included in the computation of diluted net loss per share, as the result would be anti-dilutive.
The basic and diluted net income and loss per share calculations for the three and six months ended June 30, 2010 and 2009 are as follows (in thousands, except per share data):
Three Months Ended June 30, | Six Months Ended June 30, | |||||||||||||
2010 | 2009 | 2010 | 2009 | |||||||||||
Net income (loss) | $ | 5,416 | $ | (5,267 | ) | $ | 1,380 | $ | (12,881 | ) | ||||
Weighted-average number of shares used in computing net income (loss) per share: | ||||||||||||||
Basic | 50,452 | 48,335 | 50,099 | 48,184 | ||||||||||
Diluted | 53,071 | 48,335 | 52,876 | 48,184 | ||||||||||
Net income (loss) income per share: | ||||||||||||||
Basic | $ | 0.11 | $ | (0.11 | ) | $ | 0.03 | $ | (0.27 | ) | ||||
Diluted | $ | 0.10 | $ | (0.11 | ) | $ | 0.03 | $ | (0.27 | ) | ||||
Recent Accounting Pronouncements
In October 2009, the FASB issued Accounting Standards Update (“ASU”) No. 2009-13,Revenue Recognition (Topic 605): Multiple-Deliverable Revenue Arrangements (“ASU 2009-13”) and ASU No. 2009-14,Software (Topic 985): Certain Revenue Arrangements That Include Software Elements (“ASU 2009-14”). ASU 2009-13 provides for two significant changes to the existing multiple-element revenue arrangements guidance. The first relates to the determination of when the individual deliverables included in a multiple-element arrangement may be treated as separate units of accounting. This change is significant as it will likely result in the requirement to separate more deliverables within an arrangement, ultimately leading to less revenue deferral. The second change modifies the manner in which the transaction consideration is allocated to the separately identified deliverables. ASU 2009-14 updates guidance on how entities account for revenue arrangements that contain both hardware and software elements.
We prospectively adopted ASU 2009-13 and ASU 2009-14 on January 1, 2010. We have applied ASU 2009-13 to our revenue arrangements containing multiple deliverables that were entered into or significantly modified on or after January 1, 2010. These deliverables can consist of consoles, options for the console, single-procedure disposable products, service and maintenance agreements, biomedical equipment education and exchange rights for alternative platforms of our product functionality. As a result of adopting ASU 2009-13, we have identified additional separate units of accounting related to options for our consoles, biomedical equipment education and exchange rights for alternative platforms of our product functionality. We allocate arrangement consideration based on the relative selling prices of the separate units of accounting contained within an arrangement containing multiple deliverables. Selling prices are determined using fair value, when available, or our estimate of selling price when fair value is not available for a given unit of accounting. Significant inputs in our estimates of the selling price of separate units of accounting include market and pricing trends, a customer’s geographic location and the expected gross margins by product line. Prior to the adoption of ASU 2009-13, we used the residual method to allocate the arrangement consideration when we had not established fair value of delivered items and deferred all arrangement consideration when fair value was not available for undelivered items. Typically, we complete all obligations under an arrangement with multiple deliverables within one year.
The adoption of ASU 2009-13 did not have a material impact on our consolidated financial position or results of operations as of and for the three and six month periods ending June 30, 2010. As a result of adopting ASU 2009-13, we recognized additional revenues in the three and six months ended June 30, 2010 of $468,000 and $745,000, respectively. Had we adopted ASU 2009-13 on January 1, 2009, we would have recognized additional revenues in the three and six months ended June 30, 2009 of $193,000 and $381,000, respectively.
The adoption of ASU 2009-14 did not impact our consolidated financial position or results of operations.
In February 2010, the FASB issued ASU No. 2010-09,Subsequent Events (Topic 855) which updates the guidance in ASC Topic 855,Subsequent Events, to no longer require companies that file with the SEC to indicate the date through which they have analyzed subsequent events. This updated guidance became effective immediately upon issuance.
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VOLCANO CORPORATION
NOTES TO UNAUDITED CONSOLIDATED FINANCIAL STATEMENTS—(Continued)
June 30, 2010
(Unaudited)
Reclassification
Certain reclassifications have been made to the prior year’s financial statements to conform to current year presentation.
2. Acquisitions
CardioSpectra Acquisition
On December 18, 2007, we acquired CardioSpectra, Inc. (“CardioSpectra”), a privately-held company, as a wholly-owned subsidiary of Volcano. The acquisition was accounted for as an asset purchase. We acquired all of the outstanding equity interests in CardioSpectra for $27.0 million, consisting of $25.2 million in cash, transaction costs of $1.4 million and assumed liabilities of $0.4 million. The agreement provided for additional payments up to an aggregate of $38.0 million in the event certain milestones set forth in the merger agreement are achieved. We will use commercially reasonable efforts to cause the milestones to occur. The milestone payments are payable, at our sole discretion, in cash, shares of our common stock, or a combination of both, and will be accounted for if and when the milestone payments become payable. In December 2009, the first milestone specified in the merger agreement was achieved, and at December 31, 2009, the corresponding payment totaling $11.0 million was recorded in accrued expenses and other current liabilities ($10.5 million) and in accounts payable ($531,000). In January 2010, we paid the milestone payment with the issuance of 609,360 shares our common stock and $531,000 of cash.
At June 30, 2010, the in-vivo testing for the OCT program is in process. The product is expected to be commercialized in early 2011. However, if we reasonably determine that a technical failure or commercial failure has occurred with respect to all or a part of the OCT program, we may, at our sole discretion, terminate all or part of the OCT cardiovascular program.
Novelis Acquisition
On May 15, 2008, we acquired all of the outstanding equity interests in Novelis, Inc. (“Novelis”), a privately-held company, which developed proprietary ultrasonic visualization and therapy technology for minimally invasive diagnostic and therapeutic devices. The core product line of Novelis is based on FL.IVUS technology. The aggregate purchase price of $12.3 million was paid in cash and included transaction costs of $204,000. In December 2009, we recorded $3.0 million of in-process research and development expense related to the probable achievement of regulatory approval for the FL.IVUS project. This represents a contractual milestone payment to be made to the former stockholders of Novelis. We expect to receive this regulatory approval in the second half of 2010.
Axsun Acquisition
On December 24, 2008, we acquired all of the outstanding equity interests in Axsun, a privately-held company that develops and manufactures optical monitors for the telecommunications industry, lasers and optical engines used in OCT imaging systems and advanced photonic components and subsystems used in spectroscopy and other industrial applications. The aggregate purchase price of $23.8 million consisted of $22.3 million paid in cash, assumed liabilities of $6.5 million, and transaction costs of $725,000, net of cash received of $5.8 million. The acquisition was accounted for as a business combination. Correspondingly, the purchase price was allocated to the net tangible and intangible assets based on their estimated fair values as of the acquisition date. Goodwill was recorded for the amount by which total purchase consideration exceeded net assets acquired. We have included the operating results associated with the Axsun acquisition in our consolidated financial statements from the date of acquisition.
Of the $22.3 million cash consideration, two escrows totaling $2.4 million were established to indemnify us and related indemnitees for certain matters, including breaches of representations and warranties and covenants included in the merger agreement for 15 months following the closing. In April 2010 we filed a claim against this escrow in relation to the LightLab litigation. (See Note 4 “Commitments and Contingencies” for additional background.) On July 16, 2010 an agreement was executed between us and Axsun under which $1.7 million of the non-appraisal rights escrow fund were released to us.
3. Financial Statement Details
Cash and Cash Equivalents and Available-for-Sale Investments
We invest our excess funds primarily in securities issued by the U.S. government, corporations, banks, municipalities, financial holding companies and in money market funds comprised of these same types of securities. Our cash and cash equivalents and available-for-sale investments are placed with high credit quality financial institutions. Additionally, we diversify our investment portfolio in order to maintain safety and liquidity and we do not hold mortgage-backed securities. As of June 30, 2010, all of our investments will mature within fourteen months. These investments are recorded at their estimated fair value with unrealized gains or losses reported as a separate component of accumulated other comprehensive loss.
ASC 820 defines fair value as an exit price that would be received from the sale of an asset or paid to transfer a liability in the principal or most advantageous market for the asset or liability in an orderly transaction between market participants on the measurement date. ASC 820 establishes a three-level hierarchy for disclosure that is based on the extent and level of judgment used to estimate the fair value of assets and liabilities.
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VOLCANO CORPORATION
NOTES TO UNAUDITED CONSOLIDATED FINANCIAL STATEMENTS—(Continued)
June 30, 2010
(Unaudited)
• | Level 1 – Valuations based on quoted prices for identical assets or liabilities in active markets at the measurement date. Since valuations are based on quoted prices that are readily and regularly available in an active market, valuation of these products does not entail a significant degree of judgment. Our Level 1 assets consist of money market funds and U.S. Treasury and agency debt securities. |
• | Level 2 – Valuations based on quoted prices for similar assets and liabilities in active markets; quoted prices for identical or similar assets and liabilities in markets that are not active; or other inputs that are observable or can be corroborated by observable market data, such as alternative pricing sources with reasonable levels of price transparency. Our Level 2 assets consist of corporate debt securities including commercial paper, corporate bonds, certificates of deposit and foreign exchange forward contracts. |
• | Level 3 – Valuations based on inputs that are unobservable and significant to the overall fair value measurement. We have not measured the fair value of any of our assets using Level 3 inputs. |
We utilize a third-party pricing service to assist us in obtaining fair value pricing for our investments. Pricing for Level 2 securities is based on proprietary models. Inputs are documented in accordance with the fair value disclosure hierarchy. During the three and six months ended June 30, 2010, no transfers were made into or out of the Level 3 categories. We review our fair value inputs on a quarterly basis.
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VOLCANO CORPORATION
NOTES TO UNAUDITED CONSOLIDATED FINANCIAL STATEMENTS—(Continued)
June 30, 2010
(Unaudited)
The fair value of our financial assets subject to the disclosure requirements of ASC 820 was determined using the following levels of inputs at June 30, 2010 and December 31, 2009 (in thousands):
Fair Value Measurements at June 30, 2010 | ||||||||||||
Total | Level 1 | Level 2 | Level 3 | |||||||||
Assets: | ||||||||||||
Current: | ||||||||||||
Cash | $ | 13,001 | $ | 13,001 | $ | — | $ | — | ||||
Money market funds | 32,900 | 32,900 | — | — | ||||||||
Corporate debt securities | 33,402 | — | 33,402 | — | ||||||||
U.S. Treasury and agency debt securities | 48,295 | 48,295 | — | — | ||||||||
Total | $ | 127,598 | $ | 94,196 | $ | 33,402 | $ | — | ||||
Long Term: | ||||||||||||
Corporate debt securities | 3,788 | — | 3,788 | — | ||||||||
Total Assets | $ | 131,386 | $ | 94,196 | $ | 37,190 | $ | — | ||||
Liabilities: | ||||||||||||
Foreign exchange forward contracts | $ | 24 | $ | — | $ | 24 | $ | — | ||||
The Company determines the appropriate balance sheet classification of its investments in debt securities based on maturity date at the time of purchase and evaluates the classification at each balance sheet date. The amortized cost of debt securities is adjusted for amortization of premiums and accretion of discounts to maturity value. Such amortization and accretion are included in interest income.
Fair Value Measurements at December 31, 2009 | ||||||||||||
Total | Level 1 | Level 2 | Level 3 | |||||||||
Assets: | ||||||||||||
Cash | $ | 11,255 | $ | 11,255 | $ | — | $ | — | ||||
Money market funds | 44,800 | 44,800 | — | — | ||||||||
Corporate debt securities | 37,707 | — | 37,707 | — | ||||||||
U.S. Treasury and agency debt securities | 28,321 | 28,321 | — | — | ||||||||
Foreign exchange forward contracts | 190 | — | 190 | — | ||||||||
$ | 122,273 | $ | 84,376 | $ | 37,897 | $ | — | |||||
Short-term and long-term investments have been classified as available-for-sale investments. At June 30, 2010, available-for-sale investments are detailed as follows (in thousands):
Amortized Cost | Gross Unrealized Gains | Gross Unrealized Losses | Estimated Fair Value | |||||||||
Corporate debt securities | $ | 28,686 | $ | — | $ | 11 | $ | 28,675 | ||||
U.S. Treasury and agency debt securities | 48,286 | 13 | 4 | 48,295 | ||||||||
Short-term available-for-sale investments | $ | 76,972 | $ | 13 | $ | 15 | $ | 76,970 | ||||
Corporate debt securities | 3,800 | — | 12 | 3,788 | ||||||||
Long-term available for sale investments | $ | 3,800 | $ | — | $ | 12 | $ | 3,788 | ||||
At June 30, 2010, approximately $20.8 million of our corporate debt securities were in an unrealized loss position.
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VOLCANO CORPORATION
NOTES TO UNAUDITED CONSOLIDATED FINANCIAL STATEMENTS—(Continued)
June 30, 2010
(Unaudited)
At December 31, 2009, available-for-sale investments are detailed as follows (in thousands):
Amortized Cost | Gross Unrealized Gains | Gross Unrealized Losses | Estimated Fair Value | |||||||||
Corporate debt securities | $ | 37,704 | $ | 9 | $ | 6 | $ | 37,707 | ||||
U.S. Treasury and agency debt securities | 28,330 | 16 | 25 | 28,321 | ||||||||
$ | 66,034 | $ | 25 | $ | 31 | $ | 66,028 | |||||
Derivative Financial Instruments
Our derivative financial instruments are composed entirely of foreign exchange forward contracts. We record derivative financial instruments as either assets or liabilities in our consolidated balance sheets and measure them at fair value. At June 30, 2010 and December 31, 2009, notional amounts of our outstanding contracts were $35.8 million and $24.2 million, respectively. At June 30, 2010 and December 31, 2009, the outstanding derivatives had maturities of 92 days or less. The fair value of our foreign exchange forward contracts of $24,000 was included in accrued expenses and other current liabilities in our consolidated balance sheet at June 30, 2010, and the fair value of our foreign exchange forward contracts of $190,000 was included in prepaid expenses and other current assets in our consolidated balance sheet at December 31, 2009. For the three and six months ended June 30, 2010, $370,000 of net losses and $109,000 of net gains, respectively, related to our derivative financial instruments are included in exchange rate loss in our consolidated statements of operations. Our use of derivative financial instruments commenced in October 2009, therefore no such gains or losses were recorded in any other period presented.
Inventories
Inventories consist of the following (in thousands):
June 30, 2010 | December 31, 2009 | |||||
Finished goods | $ | 12,741 | $ | 10,985 | ||
Work-in-process | 10,401 | 9,374 | ||||
Raw materials | 16,103 | 17,351 | ||||
$ | 39,245 | $ | 37,710 | |||
Intangible Assets
Intangible assets consist of developed technology, licenses, customer relationships, patents and trademarks, and assembled workforce, which are amortized using the straight-line method over periods ranging from three to ten years, representing the estimated useful lives of the assets.
During the three and six months ended June 30, 2010, we recorded intangible asset additions of approximately $100,000 and $2.2 million, respectively, primarily for purchased developed technology.
At June 30, 2010, intangible assets subject to amortization, by major class, consist of the following (in thousands):
June 30, 2010 | |||||||||||
Cost | Accumulated Amortization | Net | Weighted- Average Life (in years) (1) | ||||||||
Developed technology | $ | 22,501 | $ | 13,990 | $ | 8,511 | 8.2 | ||||
Licenses | 7,034 | 5,074 | 1,960 | 10.0 | |||||||
Customer relationships | 2,554 | 1,864 | 690 | 6.4 | |||||||
Patents and trademarks | 2,365 | 1,068 | 1,297 | 7.2 | |||||||
Assembled workforce | 274 | 172 | 102 | 4.0 | |||||||
$ | 34,728 | $ | 22,168 | $ | 12,560 | 8.3 | |||||
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VOLCANO CORPORATION
NOTES TO UNAUDITED CONSOLIDATED FINANCIAL STATEMENTS—(Continued)
June 30, 2010
(Unaudited)
At December 31, 2009, intangible assets subject to amortization, by major class, consist of the following (in thousands):
December 31, 2009 | |||||||||||
Cost | Accumulated Amortization | Net | Weighted- Average Life (in years) (1) | ||||||||
Developed technology | $ | 20,565 | $ | 13,382 | $ | 7,183 | 7.3 | ||||
Licenses | 7,034 | 4,747 | 2,287 | 10.0 | |||||||
Customer relationships | 2,473 | 1,788 | 685 | 6.7 | |||||||
Patents and trademarks | 2,231 | 900 | 1,331 | 6.9 | |||||||
Assembled workforce | 274 | 137 | 137 | 4.0 | |||||||
$ | 32,577 | $ | 20,954 | $ | 11,623 | 7.6 | |||||
(1) | Weighted average life of intangible assets is presented excluding fully amortized assets. |
At June 30, 2010, future amortization expense associated with our intangible assets is expected to be as follows (in thousands):
2010 (remaining six months) | $ | 1,295 | |
2011 | 2,509 | ||
2012 | 2,426 | ||
2013 | 2,095 | ||
2014 | 1,455 | ||
Thereafter | 2,780 | ||
$ | 12,560 | ||
Accrued Warranty
We typically offer a one-year warranty for parts and labor on our products commencing upon the transfer of title and risk of loss to the customer. We accrue the estimated cost of product warranties when we invoice our customers, based on historical results. The warranty obligation is affected by product failure rates, material usage and service delivery costs incurred in correcting a product failure. Should actual product failure rates, material usage or service delivery costs differ from these estimates, revisions to the estimated warranty liability would be required. We periodically assess the adequacy of our recorded warranty liabilities and adjust the amounts as necessary.
Accrued warranty liability is included in accrued expenses and other current liabilities in the unaudited consolidated balance sheets. The change in the accrued warranty liability for the six months ended June 30, 2010 and 2009 is summarized in the following table (in thousands):
Six Months Ended June 30, | ||||||||
2010 | 2009 | |||||||
Balance at beginning of period | $ | 1,159 | $ | 1,104 | ||||
Warranties issued | 655 | 990 | ||||||
Settlements | (898 | ) | (1,034 | ) | ||||
Balance at end of period | $ | 916 | $ | 1,060 | ||||
Restructuring Activity
In June 2009, we implemented a restructuring plan to consolidate our resources related to the research and development of our OCT technology. As part of the restructuring plan, during the first quarter of 2010 we completed the closure of our San Antonio, Texas facility and relocated such operations to our Billerica, Massachusetts facility. Approximately 20 employees were impacted by the restructuring plan. One-time benefits to affected employees included relocation or a separation agreement including severance payments, continuing medical benefits, and outplacement assistance. At March 31, 2010, 16 employees had entered into separation agreements. Service requirements vary under each separation agreement and all terminations were completed as of May 31, 2010.
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VOLCANO CORPORATION
NOTES TO UNAUDITED CONSOLIDATED FINANCIAL STATEMENTS—(Continued)
June 30, 2010
(Unaudited)
We have accounted for the restructuring plan in accordance with FASB ASC Topic 420,Exit or Disposal Cost Obligations (“ASC 420”). Consistent with ASC 420 we accrued relocation costs and the costs of one-time termination benefits to employees who were not required to render service beyond a minimum retention period of 60 days. The remaining one-time termination benefits were recorded to expense ratably over required service periods. Additionally, costs related to moving equipment between the facilities were expensed during the period incurred. As a result, we recorded $63,000 as research and development expense during the six months ended June 30, 2010. In addition, during the first quarter of 2010 we recorded $454,000 of additional restructuring costs as selling, general and administrative expense for the termination of the operating lease and related contract costs, and a charge for the impairment of certain property and equipment.
On April 26, 2010, we entered into a lease termination agreement with the landlord of our San Antonio facility. Total termination costs of $330,000 included a lump-sum lease-termination payment, broker commissions and the surrender of our security deposit. We are correspondingly released from any future obligations under this facility lease. The termination payment represented a savings over the original estimated restructuring liability related to the remaining lease payments and resulted in a benefit of $116,000 that was recorded during the second quarter.
At June 30, 2010, our restructuring liability included in accrued expenses and other current liabilities of our unaudited consolidated balance sheets (in thousands) is detailed as follows:
Relocation | One time termination benefits | Facility moving costs | Operating lease commitments | Impairment of property and equipment | Total | |||||||||||||||||||
Liability as of December 31, 2009 | $ | 56 | $ | 99 | $ | — | $ | — | $ | — | $ | 155 | ||||||||||||
Additions | — | 34 | 29 | 446 | 8 | 517 | ||||||||||||||||||
Non-cash charges | — | — | — | — | (8 | ) | (8 | ) | ||||||||||||||||
Cash payments | (56 | ) | (93 | ) | (11 | ) | — | — | (160 | ) | ||||||||||||||
Liability as of March 31, 2010 | $ | — | $ | 40 | $ | 18 | $ | 446 | $ | — | $ | 504 | ||||||||||||
Reversals | — | — | — | (116 | ) | — | (116 | ) | ||||||||||||||||
Cash payments | — | (25 | ) | (18 | ) | (330 | ) | — | (373 | ) | ||||||||||||||
Liability as of June 30, 2010 | $ | — | $ | 15 | $ | — | $ | — | $ | — | $ | 15 | ||||||||||||
Debt and Credit Facilities
The amounts outstanding for long-term debt relate to capital leases at June 30, 2010 and December 31, 2009.
4. Commitments and Contingencies
Litigation – LightLab
On January 7, 2009, LightLab Imaging, Inc. (“LightLab”) filed a complaint against us and our wholly-owned subsidiary, Axsun, in the Superior Court of Massachusetts, Suffolk County, seeking injunctive relief and unspecified damages (the “Massachusetts Action”). LightLab develops and sells OCT products for cardiovascular imaging and other medical uses. On July 6, 2010, LightLab was acquired by St. Jude Medical, Inc. (“St. Jude”).
Prior to our acquisition of Axsun, Axsun had entered into a development and supply agreement (the “Agreement”) with LightLab, in which, among other things, Axsun agreed to supply tunable lasers to LightLab for use in LightLab’s OCT imaging products until April 2016, with exclusivity in the field of coronary artery imaging expiring in April 2014. Since the acquisition, Axsun has continued to supply lasers to LightLab. The complaint includes allegations that Volcano interfered with the Agreement and with LightLab’s advantageous business relationship with Axsun, that Axsun breached the Agreement, that Axsun and Volcano misappropriated LightLab’s confidential information and trade secrets, and violated Chapter 93A, a Massachusetts statute that provides for recovery of up to three times damages plus attorneys fees (“M.G.L. c. 93A”).
The Judge ordered that the trial in the Massachusetts Action proceed in separate phases, with a jury trial first on liability, followed by a jury trial on damages, and then non-jury hearings on liability under M.G.L. c. 93A and on injunctive relief. The jury trial on liability commenced on January 4, 2010 and the jury returned a verdict on February 4, 2010 that included findings that the contract specification for the laser Axsun supplies to LightLab is a trade secret of LightLab, that Axsun agreed not to sell any tunable lasers for use in cardiology imaging to any third party during the exclusivity period in the contract, and that Axsun breached its contract with LightLab. The jury further found that Volcano intentionally interfered with LightLab’s advantageous business relationship with Axsun.
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VOLCANO CORPORATION
NOTES TO UNAUDITED CONSOLIDATED FINANCIAL STATEMENTS—(Continued)
June 30, 2010
(Unaudited)
A trial in the Massachusetts Action with respect to damages was set to commence on April 7, 2010 (“Damages Trial”). In lieu of conducting the Damages Trial, the parties agreed and stipulated that the sum of $200,000 would be treated as if it were the jury’s verdict against the defendants in the Damages Trial (the “Stipulation”).
Upon the entry of the Stipulation, LightLab waived its rights, if any, to make any additional claims for special damages relating to lasers received in 2009 that do not meet the version 6 specification, for special damages claimed by LightLab in prior pleadings, and for the repair and/or replacement of any of the lasers specified in the Stipulation. In addition, Axsun waived its rights, if any, to make any claim for recovery from LightLab certain engineering charges in connection with a development and supply agreement with LightLab, and for return by LightLab of any of the lasers specified in the Stipulation.
Under the Stipulation, all parties expressly reserved their otherwise properly preserved rights of appeal. These rights include LightLab’s appellate rights, if any, regarding its claim for alleged lost profits in excess of the above-referenced $200,000 stipulated amount to the extent LightLab is able to establish that it has properly preserved such rights.
The injunctive relief phase of the Massachusetts Action commenced on April 12, 2010. The non-jury trial relates to LightLab’s claims for injunctive relief with respect to other alleged trade secrets and is ongoing. The trial is not yet complete, and no decision has been issued. In addition, no decision has been issued with respect to LightLab’s claim under M.G.L. c. 93A to recover up to three times damages plus attorneys fees, or on injunctive relief.
Additionally, on February 5, 2010, Volcano and its wholly-owned subsidiary, Axsun, commenced an action in the Delaware Chancery Court against LightLab seeking a declaration of Volcano and Axsun’s rights with respect to certain OCT technology, the High Definition Swept Source. The complaint was served on LightLab on March 19, 2010. LightLab then filed a counter-claim that included a claim against Axsun and Volcano for violations of M.G.L. c. 93A. Volcano and Axsun moved to dismiss LightLab’s M.G.L. c. 93A counter-claim, and LightLab responded to that motion by amending its M.G.L. c. 93A counter-claim.
We are not able to predict or estimate the ultimate outcome or possible losses relating to the Massachusetts Action or any of the other lawsuits, claims or counterclaims described above.
Litigation – St. Jude
On July 27, 2010, St. Jude filed a lawsuit against Volcano in federal district court in Delaware, alleging that our pressure guide wire products infringe five patents owned by St. Jude. This action does not involve OCT technology and is separate from the Massachusetts Action.
We are not able to predict or estimate the ultimate outcome or possible losses relating to this action.
Litigation – Other
We may also be a party to various other claims in the normal course of business. Legal fees and other costs associated with such actions are expensed as incurred and were not material in any period reported. Additionally, we assess, in conjunction with our legal counsel, the need to record a liability for litigation and contingencies. Reserve estimates are recorded when and if it is determined that a loss related matter is both probable and reasonably estimable. We believe that the ultimate disposition of these matters will not have a material impact on our consolidated results of operations, financial position or cash flows. Our evaluation of the likely impact of these matters could change in the future and unfavorable outcomes and/or defense costs, depending upon the amount and timing, could have a material adverse effect on results of operations or cash flows in future periods.
Operating Leases
In January 2010, we entered into a lease agreement for approximately 32,000 square feet of office space for our corporate headquarters in San Diego, California for which we are obligated to pay approximately $5.2 million of rent over a five year period commencing on August 1, 2010. The lease contains a rent escalation clause of approximately 3% per year in each of the successive years of the lease term. We also have the option to renew the lease for an additional three year period.
Rent expense for all our facilities is recognized on a straight-line basis over the minimum lease terms.
Purchase Commitments
We have obligations under non-cancelable purchase commitments. The majority of these obligations relate to inventory, primarily raw materials. At June 30, 2010, the future minimum payments under these non-cancelable purchase commitments totaled $17.5 million, all of which will require payments at various dates through January 2015.
In October 2007, we signed a clinical research support agreement with a third party in which the third party will conduct clinical studies concerning drug eluting stents. We have agreed to provide a total of $4.6 million to fund these clinical study activities. At June 30, 2010, we have a remaining obligation of up to $3.5 million and we will be billed as services are performed under the agreement. In addition, we have entered into agreements with other third parties to sponsor clinical studies. Generally, we contract with one or more clinical research sites for a single study and no one agreement is material to our consolidated results of operations or financial condition. We are usually billed as services are performed based on enrollment and are required to make payments over periods ranging from less than one year up to three years. Our actual payments under these agreements will vary based on enrollment.
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VOLCANO CORPORATION
NOTES TO UNAUDITED CONSOLIDATED FINANCIAL STATEMENTS—(Continued)
June 30, 2010
(Unaudited)
Indemnification
Our supplier, distributor and collaboration agreements generally include certain provisions for indemnification against liabilities if our products are recalled, infringe a third-party’s intellectual property rights or cause bodily injury due to alleged defects in our products. In addition, we have agreements with our present and former directors and executive officers indemnifying them against liabilities arising from service in their respective capacities to Volcano. We maintain directors’ and officers’ insurance policies that may limit our exposure to such liabilities. To date, we have not incurred any material costs as a result of such indemnifications and have not accrued any liabilities related to such obligations in the accompanying consolidated financial statements.
CardioSpectra Acquisition
In connection with our December 2007 acquisition of CardioSpectra, certain milestone payments of up to $38.0 million are payable upon achievement of milestones set forth in the merger agreement. In January 2010, we paid $11.0 million to the former stockholders of CardioSpectra with the issuance of 609,360 shares of our common stock and $531,000 of cash for achievement of the first milestone in December 2009. We may make additional payments of up to an aggregate of $27.0 million in the event that the additional milestones, as set forth in the merger agreement, are achieved. See Note 2 “Acquisitions” for additional details.
Novelis Acquisition
In connection with our May 2008 acquisition of Novelis (see Note 2 “Acquisitions”), we may make an additional cash payment of $3.0 million based on the achievement of a specific regulatory milestone. This amount was accrued during the fourth quarter of 2009 as payment was deemed probable.
5. Stockholders’ Equity
Stock Benefit Plans
Our 2005 Amended and Restated Equity Compensation Plan (“2005 Amended Plan”) provides for an aggregate of 13,712,558 shares of our common stock that may be issued or transferred to our employees, non-employee directors and consultants. Commencing July 29, 2009, the number of shares of common stock available for issuance under the 2005 Amended Plan are reduced by one share for each share of stock issued pursuant to a stock option or a stock appreciation right and one and sixty-three hundredths (1.63) shares for each share of common stock issued pursuant to a restricted stock award, restricted stock unit (“RSU”) award, performance stock award or other stock award. Shares net exercised or retained to cover a participant’s minimum tax withholding obligations do not again become available for issuance under the 2005 Amended Plan.
At June 30, 2010, we have granted stock options and RSUs under the 2005 Amended Plan. Stock options previously granted under the 2000 Long Term Incentive Plan that are cancelled or expire will increase the shares available for grant under the 2005 Amended Plan. In addition, employees have purchased shares of the Company’s common stock under the 2007 Employee Stock Purchase Plan (the “Purchase Plan”). At June 30, 2010, 2,864,554 shares and 670,523 shares remained available to grant under the 2005 Amended Plan and the Purchase Plan, respectively.
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VOLCANO CORPORATION
NOTES TO UNAUDITED CONSOLIDATED FINANCIAL STATEMENTS—(Continued)
June 30, 2010
(Unaudited)
Stock Option Activity
Stock option activity for the six months ended June 30, 2010 is as follows:
Stock Options | Weighted- Average Exercise Price | Weighted- Average Remaining Contractual Life (in years) | Aggregate Intrinsic Value (in thousands) | ||||||||
Outstanding at December 31, 2009 | 5,513,458 | $ | 11.25 | ||||||||
Granted | 783,090 | 19.21 | |||||||||
Exercised | (953,616 | ) | 7.41 | ||||||||
Forfeited or expired | (264,563 | ) | 15.79 | ||||||||
Outstanding and exercisable at June 30, 2010 | 5,078,369 | 12.96 | 4.6 | $ | 45,031 | ||||||
Vested and expected to vest at June 30, 2010 | 4,931,152 | 12.86 | 4.6 | 44,222 | |||||||
The total intrinsic value of stock options exercised during the three months ended June 30, 2010 and 2009 and six months ended June 30, 2010 and 2009 was $6.8 million, $1.6 million, $14.2 million, and $4.6 million, respectively, which represents the difference between the exercise price of the stock option and the fair value of our common stock on the dates the stock options were exercised.
Non-vested stock option activity for the six months ended June 30, 2010 is as follows:
Non-vested Stock Options | Weighted-Average Grant Date Fair Value | |||||
Outstanding at December 31, 2009 | 1,879,243 | $ | 6.64 | |||
Granted | 783,090 | 7.71 | ||||
Vested | (544,296 | ) | 7.03 | |||
Forfeited or expired | (256,105 | ) | 4.27 | |||
Outstanding at June 30, 2010 | 1,861,932 | 6.85 | ||||
The weighted-average grant date fair value of stock options granted during the three months ended June 30, 2010 and 2009 and six months ended June 30, 2010 and 2009 was $9.73, $5.66, $8.03, and $5.82, respectively.
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VOLCANO CORPORATION
NOTES TO UNAUDITED CONSOLIDATED FINANCIAL STATEMENTS—(Continued)
June 30, 2010
(Unaudited)
Restricted Stock Unit Activity
RSU activity for the six months ended June 30, 2010 is as follows:
Restricted Stock Units | |||
Outstanding at December 31, 2009 | 733,898 | ||
Granted | 324,700 | ||
Vested | (203,744 | ) | |
Forfeited or expired | (108,997 | ) | |
Outstanding at June 30, 2010 | 745,857 | ||
These time-vested RSUs entitle the holder to shares of common stock as the units vest in equal annual installments over a four-year period. The weighted-average grant-date fair value of each RSU granted during the six months ended June 30, 2010 and 2009 was $19.07 and $13.69, respectively. No RSUs were granted during the three months ended June 30, 2010 and 2009.
During the six months ended June 30, 2010, we released 201,400 shares of common stock based on the vesting terms of certain RSU agreements.
Employee Stock Purchase Plan Activity
The Purchase Plan provides eligible employees the opportunity to purchase shares of the Company’s common stock at the lower of up to 85% of the fair market value on the first or last day of the applicable offering period, by having withheld from their salary an amount up to 15% of their compensation, without paying brokerage fees or commissions on purchases. Our Purchase Plan is deemed to be compensatory, therefore Purchase Plan expense has been included in our consolidated statements of operations for the three and six months ended June 30, 2010 and 2009. We pay for the administrative expenses of the Purchase Plan. No employee may purchase more than $25,000 worth of common stock (calculated at the time the purchase right is granted) in any calendar year, nor purchase more than 750 shares in any six-month purchase period.
Commencing January 1, 2008, common stock reserved for issuance under the Purchase Plan automatically increases by the lesser of 1 1/2% of our outstanding common stock or 600,000 shares on the first day of January of each year. In November 2009, the Board of Directors exercised its right not to increase the number of shares of common stock available for issuance under the Purchase Plan that was scheduled to occur on January 1, 2010. As a result, at June 30, 2010, the number of shares of common stock reserved for issuance under the Purchase Plan remained at 1,100,000 shares.
During the six months ended June 30, 2010 and 2009, 103,141 and 78,462 shares, respectively, were purchased at a per share price of $11.96 and $12.72, respectively.
Fair Value Assumptions
The fair value of each stock option is estimated on the date of grant using the Black-Scholes-Merton option-pricing (the “Black-Scholes”) model utilizing the following weighted-average assumptions:
Three Months Ended June 30, | Six Months Ended June 30, | |||||||||||
2010 | 2009 | 2010 | 2009 | |||||||||
Risk-free interest rate | 2.6 | % | 1.9 | % | 2.4 | % | 1.9 | % | ||||
Expected life (years) | 4.5 | 4.6 | 4.6 | 5.0 | ||||||||
Estimated volatility | 46.5 | % | 47.1 | % | 47.0 | % | 45.9 | % | ||||
Expected dividends | None | None | None | None |
The risk-free interest rate for periods within the contractual life of the stock option is based on the implied yield available on U.S. Treasury constant maturity securities with the same or substantially equivalent remaining terms at the time of grant.
Since January 1, 2008, we have used our historical stock option exercise experience to estimate the expected term of our stock options.
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VOLCANO CORPORATION
NOTES TO UNAUDITED CONSOLIDATED FINANCIAL STATEMENTS—(Continued)
June 30, 2010
(Unaudited)
Estimated volatility was calculated using the historical volatility of the common stock of comparable medical device companies using weekly price observations over a period generally commensurate with the expected term of our stock options. We did not exclude any period due to discrete historical events. We use the historical volatility of similar companies due to the limited trading history of our common stock. Since the completion of our initial public offering, we have also included the weekly price observations of our common stock, weighted for the number of price observations, in our estimate of volatility. We also evaluate, at least annually, whether circumstances have changed such that the identified entities are no longer similar to us, and remove or replace the peer companies in our analysis. We will continue to assess the appropriateness of our methodology for future periods.
We use a zero value for the expected dividend value factor since we have not declared any dividends in the past and we do not anticipate declaring any dividends in the foreseeable future.
The fair value of each purchase option under the Purchase Plan is estimated at the beginning of each purchase period using the Black-Scholes model utilizing the following weighted-average assumptions:
Three Months Ended June 30, | Six Months Ended June 30, | |||||||||||||||
2010 | 2009 | 2010 | 2009 | |||||||||||||
Risk-free interest rate | 0.2 | % | 0.5 | % | 0.2 | % | 1.0 | % | ||||||||
Expected life (years) | 0.5 | 0.5 | 0.5 | 0.5 | ||||||||||||
Estimated volatility | 32.6 | % | 77.1 | % | 36.6 | % | 67.1 | % | ||||||||
Expected dividends | None | None | None | None | ||||||||||||
Fair value of purchase right | $ | 5.10 | $ | 4.99 | $ | 4.69 | $ | 5.08 |
The computation of the expected volatility assumption used in the Black-Scholes model for purchase rights is based on the trading history of our common stock. The expected life assumption is based on the six-month term of each offering period. The risk-free interest rate is based on U.S. Treasury constant maturity securities with the same or substantially equivalent remaining term in effect at the beginning of the offering period. We use a zero value for the expected dividend value factor since we have not declared any dividends in the past and we do not anticipate declaring any dividends in the foreseeable future.
We estimate forfeitures and only recognize expense for those shares expected to vest. Our estimated forfeiture rates in the three and six months ended June 30, 2010 and 2009 are based on our historical forfeiture experience.
Stock-Based Compensation Expense
The following table sets forth stock-based compensation expense included in our consolidated statements of operations (in thousands):
Three Months Ended June 30, | Six Months Ended June 30, | |||||||||||
2010 | 2009 | 2010 | 2009 | |||||||||
Cost of revenues | $ | 198 | $ | 174 | $ | 401 | $ | 385 | ||||
Selling, general and administrative | 2,522 | 2,308 | 5,060 | 4,388 | ||||||||
Research and development | 388 | 368 | 730 | 792 | ||||||||
$ | 3,108 | $ | 2,850 | $ | 6,191 | $ | 5,565 | |||||
Included in our stock-based compensation expense is $166,000, $49,000, $325,000, and $103,000 of stock-based compensation expense related to non-employees in the three months ended June 30, 2010 and 2009 and the six months ended June 30, 2010 and 2009, respectively. In addition, $215,000, $266,000, $428,000, and $432,000 of stock-based compensation expense related to the Purchase Plan was recorded in the three months ended June 30, 2010 and 2009 and the six months ended June 30, 2010 and 2009, respectively. At June 30, 2010 and December 31, 2009, there was $239,000 and $265,000, respectively, of total stock-based compensation cost capitalized in inventories.
At June 30, 2010, there was $12.4 million, $12.0 million and $146,000 of total unrecognized compensation cost for stock options, RSUs and the Purchase Plan, respectively, which is expected to be recognized over weighted average terms of 2.6 years, 2.9 years and 0.2 years, respectively.
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VOLCANO CORPORATION
NOTES TO UNAUDITED CONSOLIDATED FINANCIAL STATEMENTS—(Continued)
June 30, 2010
(Unaudited)
Accumulated Other Comprehensive Loss
The following table summarizes the components of our accumulated other comprehensive loss (in thousands):
June 30, 2010 | December 31, 2009 | |||||||
Net unrealized loss on available-for-sale investments | $ | (14 | ) | $ | (6 | ) | ||
Accumulated foreign currency translation adjustments | (3,515 | ) | (4,073 | ) | ||||
$ | (3,529 | ) | $ | (4,079 | ) | |||
6. Segment and Geographic Information
Our chief operating decision-maker reviews financial information presented on a consolidated basis, accompanied by disaggregated information about segment revenues by product and geographic region for purposes of making operating decisions and assessing financial performance. Historically, we considered ourselves to be a single reporting segment, specifically the manufacture, sale, discovery, development and commercialization of products for the diagnosis of atherosclerosis in the coronary arteries and peripheral vascular system (“Medical Segment”). In connection with our acquisition of Axsun in December 2008, we operate an additional segment, specifically the discovery, development, manufacture and sale of micro-optical spectrometers and optical channel monitors to telecommunications and other industrial companies (“Industrial Segment”, formerly referred to as our “Telecommunications”, or “Telecom”, Segment).
We do not assess the performance of our segments on other measures of income or expense, such as depreciation and amortization, operating income or net income. We do not produce reports for, or measure the performance of, our segments on any asset-based metrics. Therefore, segment information is presented only for revenues by product.
The following table sets forth our revenues by segment and product expressed as dollar amounts (in thousands) and the changes in revenues between the specified periods expressed as percentages:
Three Months Ended June 30, | Percentage Change | Six Months Ended June 30, | Percentage Change | |||||||||||||||
2010 | 2009 | 2009 to 2010 | 2010 | 2009 | 2009 to 2010 | |||||||||||||
Medical segment: | ||||||||||||||||||
Consoles | $ | 10,796 | $ | 9,317 | 15.9 | % | $ | 19,456 | $ | 17,813 | 9.2 | % | ||||||
Single-procedure disposables: | ||||||||||||||||||
IVUS | 40,931 | 31,808 | 28.7 | 79,481 | 60,352 | 31.7 | ||||||||||||
FM | 10,752 | 7,209 | 49.1 | 21,304 | 13,469 | 58.2 | ||||||||||||
Other | 4,317 | 2,089 | 106.7 | 7,995 | 4,370 | 83.0 | ||||||||||||
Sub-total medical segment | 66,796 | 50,423 | 32.5 | 128,236 | 96,004 | 33.6 | ||||||||||||
Industrial segment | 6,656 | 3,619 | 83.9 | 11,788 | 6,997 | 68.5 | ||||||||||||
$ | 73,452 | $ | 54,042 | 35.9 | $ | 140,024 | $ | 103,001 | 35.9 | |||||||||
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VOLCANO CORPORATION
NOTES TO UNAUDITED CONSOLIDATED FINANCIAL STATEMENTS—(Continued)
June 30, 2010
(Unaudited)
The following table sets forth our revenues by geography expressed as dollar amounts (in thousands) and the changes in revenues in the specified periods expressed as percentages:
Three Months Ended June 30, | Percentage Change | Six Months Ended June 30, | Percentage Change | |||||||||||||||
2010 | 2009 | 2009 to 2010 | 2010 | 2009 | 2009 to 2010 | |||||||||||||
Revenues (1): | ||||||||||||||||||
United States | $ | 33,948 | $ | 26,641 | 27.4 | % | $ | 62,904 | $ | 50,851 | 23.7 | % | ||||||
Japan | 18,623 | 11,776 | 58.1 | 36,720 | 23,460 | 56.5 | ||||||||||||
Europe, the Middle East and Africa | 15,016 | 11,738 | 27.9 | 29,123 | 21,374 | 36.3 | ||||||||||||
Rest of world | 5,865 | 3,887 | 50.9 | 11,277 | 7,316 | 54.1 | ||||||||||||
$ | 73,452 | $ | 54,042 | 35.9 | $ | 140,024 | $ | 103,001 | 35.9 | |||||||||
(1) | Revenues are attributed to geographies based on the location of the customer, except for shipments to original equipment manufacturers, which are attributed to the country of the origin of the equipment distributed. |
At June 30, 2010, approximately 60% of our property, plant, and equipment, net are located in the U.S., approximately 33% are located in Japan, and less than 10% are located in our remaining geographies.
7. Income Taxes
We are subject to taxation in the U.S. and various state and foreign jurisdictions. We record liabilities for income tax contingencies based on our best estimate of the underlying exposures. We are open for audit by the U.S. Internal Revenue Service and state tax jurisdictions from our inception in 2000 through 2010. We were audited by the Belgian tax authorities for the 2005 and 2006 years. There were no significant adjustments as a result of this audit. We continue to be open for audit by Belgium and various European tax jurisdictions from the inception of Volcano Europe in 2003 through 2010, and by South Africa from the inception of Volcano South Africa in 2008 through 2010. We were audited by the Japanese tax authorities for the 2005 through 2007 years. There were no significant adjustments as a result of this audit. We continue to be open for audit by the Japanese tax authorities from the inception of Volcano Japan in 2004 through 2010.
Our effective tax rate is a blended rate resulting from the composition of taxable income or loss in the various global jurisdictions in which we conduct business. Our effective tax rate excludes those jurisdictions that both continue to maintain full valuation allowances and for which we project no current year tax liabilities. We record a full valuation allowance against our deferred tax assets in the jurisdictions where we continue to incur net operating losses.
For the three months ended June 30, 2010 and 2009 and the six months ended June 30, 2010 and 2009 we recorded a provision for income taxes of approximately $253,000, $518,000, $628,000, and $712,000, respectively.
We apply the “with and without method — direct effects only”, prescribed under FASB ASC 740,Income Taxes, with respect to recognition of stock option excess tax benefits within stockholders’ equity (paid in capital). Therefore, the aforementioned provision for income tax is determined utilizing projected federal and state taxable income before the application of deductible excess tax benefits attributable to stock option exercises.
8. Subsequent Events
On August 5, 2010, we acquired all of the outstanding equity interests in Fluid Medical, Inc. (“Fluid”), a privately-held company, which is engaged in the development of imaging technology for use in various structural heart applications, including, but not limited to, mitral valve repair. The purchase price of approximately $4.2 million in cash excludes transaction costs which have not yet been finalized. We will not assume any of Fluid’s debts in relation to this transaction.
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Item 2. | Management’s Discussion and Analysis of Financial Condition and Results of Operations |
This quarterly report on Form 10-Q contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, particularly statements that may relate to, but are not limited to, expectations of future operating results or financial performance, capital expenditures, introduction of new products, regulatory compliance, plans for growth and future operations, as well as assumptions relating to the foregoing. Forward-looking statements are inherently subject to risks and uncertainties, some of which cannot be predicted or quantified. These risks and other factors include, but are not limited to, those listed under Part II, Item 1A — “Risk Factors” and elsewhere in this report. In some cases, you can identify forward-looking statements by terminology such as “may,” “will,” “should,” “could,” “expect,” “plan,” “anticipate,” “believe,” “estimate,” “predict,” “intend,” “potential,” “continue” or the negative of these terms or other comparable terminology. These statements are only predictions. Actual events or results may differ materially and adversely.
Overview
We design, develop, manufacture and commercialize a broad suite of intravascular ultrasound, or IVUS, and functional measurement, or FM, products. We believe that these products enhance the diagnosis and treatment of vascular heart disease by improving the efficiency and efficacy of existing percutaneous interventional, or PCI, therapy procedures in the coronary or peripheral arteries. We market our products to physicians and technicians who perform PCI procedures in hospitals and to other personnel who make purchasing decisions on behalf of hospitals.
Our products consist of multi-modality consoles which are marketed as stand-alone units or as customized units that can be integrated into a variety of hospital-based interventional surgical suites called catheterization laboratories, or cath labs. We have developed customized cath lab versions of these consoles and are developing additional functionality options as part of our cath lab integration initiative. Our consoles have been designed to serve as a multi-modality platform for our phased array and rotational IVUS catheters, fractional flow reserve, or FFR, pressure wires and Medtronic’s Pioneer reentry device. We are developing additional offerings for integration into the platform, including, forward-looking IVUS, or FL.IVUS, catheters, image-guided therapy catheters and ultra-high resolution Optical Coherence Tomography, or OCT, systems and catheters.
Our IVUS products include single-procedure disposable phased array and rotational IVUS imaging catheters and additional functionality options such as virtual histology IVUS tissue characterization and ChromaFlo stent apposition analysis. Our FM offerings include FM consoles and single-procedure disposable pressure and flow guide wires used to measure the pressure and flow characteristics of blood around plaque, enabling physicians to gauge the plaque’s physiological impact on blood flow and pressure.
We also develop and manufacture optical monitors, lasers, and optical engines used in OCT imaging systems as well as micro-optical spectrometers and optical channel monitors used in telecommunications and other industrial companies.
We have corporate infrastructure in the U.S., Europe and Japan; direct sales capabilities in the U.S.; and a combination of direct sales capabilities and distribution relationships in our primary international markets, including Japan, Europe, the Middle East, Canada, Asia Pacific and Latin America. Our corporate office is located in San Diego, California. Our worldwide manufacturing and research and development operations are located in Rancho Cordova, California. We also have additional research and development facilities in Cleveland, Ohio, Forsyth County, Georgia and San Diego, California. We have sales offices in Alpharetta, Georgia and Tokyo, Japan; sales and distribution offices in Zaventem, Belgium and Woodmead, South Africa; and third-party distribution facilities in Chiba, Japan and Tokyo, Japan. In addition, we have facilities in Billerica, Massachusetts for the manufacturing and operations of Axsun Technologies, Inc., or Axsun, our wholly owned subsidiary, and the research and development of OCT and FL.IVUS technology. During the first half of 2010, we completed our restructuring plan to close our facility in San Antonio, Texas and consolidated our OCT resources into our Billerica, Massachusetts facility. For details, see Note 3 to our unaudited consolidated financial statements, “Financial Statement Details – Restructuring Activity.”
We have focused on building our domestic and international sales and marketing infrastructure to market our products to physicians and technicians who perform PCI procedures in hospitals and to other personnel who make purchasing decisions on behalf of hospitals. At June 30, 2010, we had approximately 1,036 employees worldwide, including approximately 433 manufacturing employees, 285 sales and marketing employees and 129 research and development employees. We sell our products directly to customers in certain European markets and utilize distributors in other European markets, including Spain, Portugal and parts of Italy. Beginning in the third quarter of 2009, we primarily sell our products directly to customers in Japan. We also have direct contractual relationships with Fukuda Denshi Co., Ltd., or Fukuda, and Johnson & Johnson K.K., Cordis Division, or Johnson & Johnson, through which our IVUS products are distributed in Japan. In certain markets, including the major markets of Asia Pacific, Latin America, Europe, Australia, Africa and the Middle East, we have distributor relationships through which we sell our products. Our distributors are involved in product launch planning, education and training, physician support and clinical trial management.
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In the six months ended June 30, 2010 and 2009, 42.8% and 35.4%, respectively, of our revenues and 23.2% and 20.5%, respectively, of our operating expenses were denominated in various non-U.S. dollar currencies, primarily the euro and the yen. We expect that a significant portion of our revenue and operating expenses will continue to be denominated in non-U.S. dollar currencies. As a result, we are subject to risks related to fluctuations in foreign currency exchange rates, which could affect our operating results in the future.
At June 30, 2010, we had a worldwide installed base of over 5,400 consoles. We intend to grow and leverage this installed base to drive recurring sales of our single-procedure disposable catheters and guide wires. In the six months ended June 30, 2010, the sale of our single-procedure disposable catheters and guide wires accounted for $100.8 million, or 72.0% of our revenues, a $27.0 million, or 36.5% increase from the same period in 2009, in which the sale of our single-procedure disposable catheters and guide wires accounted for $73.8 million, or 71.7% of our revenues.
We manufacture our IVUS and FM consoles, IVUS catheters and FM guide wires at our facility in Rancho Cordova, California. We use third-party manufacturing partners to produce circuit boards and mechanical sub-assemblies used in the manufacture of our consoles. We also use third-party manufacturing partners for certain proprietary components used in the manufacture of our single-procedure disposable products. We perform incoming inspection on these circuit boards, mechanical sub-assemblies and components, assemble them into finished products, and test the final product to assure quality control.
On December 18, 2007, we acquired CardioSpectra, Inc., or CardioSpectra. As a result, we are developing innovative OCT technology, which is expected to complement our existing product offerings and further enhance our position as an imaging technology leader in the field of interventional medicine. OCT technology enables high resolution imaging of highly detailed structures in the vasculature, including vessel wall defects, intra-luminal thrombus and stent struts. Our long term goal is to integrate this OCT functionality into our s5 family of imaging products.
On May 15, 2008, we acquired Novelis, Inc., or Novelis, a company with proprietary ultrasonic visualization and therapy technology for minimally invasive diagnostic and therapeutic devices. Our acquisition of Novelis’ proprietary FL.IVUS technology platform is expected to help us build upon our existing suite of products and further enhance our position as an imaging technology leader in the field of interventional medicine by developing FL.IVUS and associated therapies in the interventional cardiology market. We expect to add these products and capabilities onto our s5 family of imaging products.
On December 24, 2008, we acquired Axsun Technologies, Inc., or Axsun, a company that develops and manufactures optical monitors for telecommunications, lasers and optical engines used in medical OCT imaging systems and advanced photonic components and sub-systems used in spectroscopy and other industrial applications. We believe Axsun’s proprietary OCT technology will provide us competitive advantages in the invasive imaging sector. In connection with the Axsun acquisition, we and Axsun were sued by LightLab Imaging, Inc., or LightLab. LightLab was a wholly owned subsidiary of Goodman Company, Ltd., or Goodman, which was a distributor of our IVUS and FM products in Japan until that relationship was terminated in July 2009. LightLab was acquired by St. Jude Medical, Inc., or St. Jude, on July 6, 2010. LightLab develops and sells OCT products for cardiovascular imaging and other medical uses. For details related to the litigation, see Note 4 to our unaudited consolidated financial statements, “Commitments and Contingencies – Litigation.”
Economic conditions have been depressed in many countries and regions, including without limitation the U.S., Japan, Europe, Middle East and Africa, where we have generated most of our revenues. These conditions may remain depressed for the foreseeable future. If our customers do not obtain or do not have access to the necessary capital to operate their businesses, or are otherwise adversely affected by the depressed national and worldwide economic conditions, including governments’ ability to meet their debt obligations, this could result in reductions in the sales of our products, longer sales cycles and slower adoption of new technologies by our customers, which would materially and adversely affect our business. In addition, our customers’ and suppliers’ liquidity, capital resources and credit may be adversely affected by the current financial and credit crisis, which could adversely affect our ability to collect on our outstanding invoices and lengthen our collection cycles, or limit our timely access to important sources of raw materials necessary for the manufacture of our consoles and catheters. There can be no assurances that government responses to the disruptions in the financial or credit markets will improve the national and worldwide economic conditions in the near term.
Financial Operations Overview
The following is a description of the primary components of our revenues and expenses.
Revenues. We derive our revenues from two reporting segments: medical and industrial (formerly referred to as “telecommunications” or “telecom”). Our medical segment represents our core business, in which we derive revenues primarily from the sale of our consoles and single-procedure disposables. Our industrial segment derives revenues related to the sales of Axsun’s micro-optical spectrometers and optical channel monitors to telecommunication and other industrial companies. In the six months ended June 30, 2010, we generated $140.0 million of revenues which is composed of $128.2 million from our medical segment and $11.8 million from our industrial segment. In the six months ended June 30, 2010, 15.2% of our medical segment revenues were derived from the sale of our consoles, as compared with 18.6% in the six months ended June 30, 2009. In the six months ended June 30, 2010, IVUS single-procedure disposables accounted for 62.0% of our medical segment revenues, compared to 62.9% during the same period in 2009, while in the six months ended June 30, 2010, 16.6% of our medical segment revenues were derived from the sale of our FM single-procedure disposables, as compared with 14.0% in the six months ended June 30, 2009. Other revenues consist primarily of service and maintenance revenues, rental revenues, shipping and handling revenues, sales of distributed products, spare parts sales, and license fees.
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We expect to continue to experience variability in our quarterly revenues from console sales due in part to the timing of hospital capital equipment purchasing decisions. Further, we expect variability of our revenues based on the timing of our new product introductions, which may cause our customers to delay their purchasing decisions until the new products are commercially available. Alternatively, we may include in our arrangements with customers future deliverables, such as unspecified hardware upgrades or biomedical equipment education. In these cases, we would be required to defer the allocated arrangement consideration based on the relative estimated selling prices of the undelivered items until we have met our future deliverables obligation.
Our medical segment sales in the U.S. are generated by our direct sales representatives and our products are shipped to customers throughout the U.S. from our facilities in Rancho Cordova, California and Billerica, Massachusetts. Our medical segment international sales are generated by our direct sales representatives or through independent distributors and are shipped throughout the world from our facilities in Rancho Cordova, California; Billerica, Massachusetts; Zaventem, Belgium; Chiba, Japan; Tokyo, Japan; and Woodmead, South Africa. Our industrial segment sales are generated by our direct sales representatives or through independent distributors and these products are shipped primarily to telecommunications and industrial companies domestically and abroad from our facility in Billerica, Massachusetts.
Cost of Revenues. Cost of revenues consists primarily of material costs for the products that we sell and other costs associated with our manufacturing process, such as personnel costs, rent, depreciation and utilities. In addition, cost of revenues includes depreciation of company-owned consoles, royalty expenses for licensed technologies included in our products, service costs, provisions for warranty, distribution, freight and packaging costs and stock-based compensation expense. We expect our gross margin for IVUS and FM products to improve over time if we are successful in our ongoing efforts to streamline and improve our manufacturing processes and increase production volumes.
Selling, General and Administrative. Selling, general and administrative expenses consist primarily of salaries and other related costs for personnel serving the sales, marketing, executive, finance, information technology and human resource functions. Other costs include travel and entertainment expenses, facility costs, trade show, training and other promotional expenses, professional fees for legal and accounting services and stock-based compensation expense. We expect that our selling, general and administrative expenses will increase as we continue to expand our sales force and marketing efforts and invest in the necessary infrastructure to support our continued growth.
Research and Development. Research and development expenses consist primarily of salaries and related expenses for personnel, consultants, prototype materials, clinical studies, depreciation, regulatory filing fees, certain legal costs related to our intellectual property and stock-based compensation expense. We expense research and development costs as incurred. We expect our research and development expenses to increase as we continue to develop our products, technologies and applications.
Amortization of Intangibles. Intangible assets, which consist of our developed technology, licenses, customer relationships, assembled workforce and patents and trademarks, are amortized using the straight-line method over their estimated useful lives ranging from three to ten years.
In-process Research and Development. In-process research and development, or IPR&D, consists of our projects acquired in connection with acquisitions that had not reached technological feasibility and had no alternative future uses as of each acquisition or milestone payment date. Certain additional payments that may be required in connection with our acquisitions could result in future charges to IPR&D.
In December 2007, we acquired the OCT project in connection with our acquisition of CardioSpectra, which was valued at $26.3 million. In-vivo testing and regulatory approval remained to be completed as of the acquisition date at an estimated cost of $7.2 million. In December 2009, we achieved a milestone specified in the CardioSpectra merger agreement related to the receipt of CE mark regulatory approval and $11.0 million became payable by us to the former stockholders of CardioSpectra. This amount was recorded as IPR&D expense in the year ended December 31, 2009. Although we have received CE mark approval for a preliminary version of our OCT product, this version is not intended to be commercialized. We believe there is substantial incremental effort and costs that must be incurred to complete a product that is suitable for commercialization and there is significant risk that a commercializable product may not result from our efforts. As of June 30, 2010, we estimate that we will incur $5.4 million of additional costs in order to complete the OCT project for a total of approximately $15.4 million. The OCT project was originally expected to be commercialized by late 2008; however, it was at an earlier stage of development than our initial assessment indicated. As of June 30, 2010, commercialization is not expected until early 2011. Additional milestone payments of up to $27.0 million may be paid to the former stockholders of CardioSpectra in connection with successful and timely regulatory approvals and commercialization.
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If the OCT project is not completed in a timely manner, such as if we experience delays associated with significant design changes that result from unsuccessful human trials or discoveries during human trials, we may jeopardize a potential competitive position, experience difficulties in obtaining our forecasted revenues and associated market share and we may not be required to pay some or all of the milestone payments.
In May 2008, we acquired the FL.IVUS project in connection with our acquisition of Novelis, which was valued at $12.2 million. In-vivo testing and regulatory approval protocols remained to be completed for the FL.IVUS project as of the acquisition date, at an estimated cost of $3.9 million. In December 2009, we recorded $3.0 million of additional IPR&D expense related to the probable achievement of regulatory approval for the FL.IVUS project. This represents a contractual milestone payment to be made to the former stockholders of Novelis. We expect to receive this regulatory approval in the second half of 2010. However, we believe there is significant incremental effort and costs that must be incurred to complete a product that is suitable for commercialization subsequent to the receipt of this approval. As of June 30, 2010, we estimate that we will incur $2.3 million of additional costs in order to commercialize the first product using FL.IVUS for a total of $8.2 million. We originally expected the FL.IVUS project to receive regulatory approvals and be commercialized during 2009. As of June 30, 2010, the project was behind schedule by more than one year.
If the FL.IVUS project is not completed in a timely manner, such as if we experience delays associated with significant design changes that result from unsuccessful human trials or discoveries during human trials, we may jeopardize our competitive position and experience a potential loss of revenues and associated market share and we may not be required to pay some or all of the milestone payment.
In November 2008, we acquired an IPR&D project in connection with our acquisition of Impact Medical Technologies, LLC, valued at approximately $300,000.
The following table summarizes our significant IPR&D projects (in millions):
Project Name | Fair Value | Estimated Cost to Complete, as of Acquisition Date | Costs Incurred Since Acquisition | Estimated Cost to Complete, as of June 30, 2010 | Total Estimated Costs to Complete since Acquisition Date | ||||||||||
OCT | $ | 26.3 | $ | 7.2 | $ | 10.0 | $ | 5.4 | $ | 15.4 | |||||
FL.IVUS | 12.2 | 3.9 | 5.9 | 2.3 | 8.2 |
Interest Income. Interest income is comprised of interest income earned from our cash and cash equivalents and, short-term and long-term available-for-sale investments.
Interest Expense. Interest expense is comprised primarily of interest expense related to our capital lease obligations.
Exchange Rate (Loss) Gain. Exchange rate (loss) gain is comprised of foreign currency transaction and remeasurement gains and losses, net, and the effect of changes in value and net settlements of our foreign exchange forward contracts.
Provision for Income Taxes.Our effective tax rate is a blended rate resulting from the composition of taxable income or loss in the various global jurisdictions in which we conduct business. Our effective tax rate excludes those jurisdictions that both continue to maintain full valuation allowances and project no current year tax liabilities. We record a full valuation allowance against our deferred tax assets in the jurisdictions where we continue to incur net operating losses. We apply the “with and without method — direct effects only”, prescribed under FASB ASC 740,Income Taxes, with respect to recognition of stock option excess tax benefits within stockholders equity (paid in capital). Therefore, provision for income tax is determined utilizing projected federal and state taxable income before the application of deductible excess tax benefits attributable to stock option exercises.
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Results of Operations
The following table sets forth items derived from our consolidated statements of operations for the three and six months ended June 30, 2010 and 2009, presented in both absolute dollars (in thousands) and as a percentage of revenues:
Three Months Ended June 30, | Six Months Ended June 30, | |||||||||||||||||||||||||||
2010 | 2009 | 2010 | 2009 | |||||||||||||||||||||||||
Revenues | $ | 73,452 | 100.0 | % | $ | 54,042 | 100.0 | % | $ | 140,024 | 100.0 | % | $ | 103,001 | 100.0 | % | ||||||||||||
Cost of revenues, excluding amortization of intangibles | 27,093 | 36.9 | 22,486 | 41.6 | 53,731 | 38.4 | 43,135 | 41.9 | ||||||||||||||||||||
Gross profit | 46,359 | 63.1 | 31,556 | 58.4 | 86,293 | 61.6 | 59,866 | 58.1 | ||||||||||||||||||||
Operating expenses: | ||||||||||||||||||||||||||||
Selling, general and administrative | 30,082 | 41.0 | 26,453 | 48.9 | 63,161 | 45.1 | 51,533 | 50.0 | ||||||||||||||||||||
Research and development | 9,594 | 13.1 | 9,866 | 18.3 | 19,452 | 13.9 | 18,635 | 18.1 | ||||||||||||||||||||
Amortization of intangibles | 621 | 0.8 | 1,053 | 1.9 | 1,194 | 0.9 | 2,105 | 2.1 | ||||||||||||||||||||
In-process research and development | 33 | — | — | — | 65 | — | — | — | ||||||||||||||||||||
Total operating expenses | 40,330 | 54.9 | 37,372 | 69.1 | 83,872 | 59.9 | 72,273 | 70.2 | ||||||||||||||||||||
Operating income (loss) | 6,029 | 8.2 | (5,816 | ) | (10.7 | ) | 2,421 | 1.7 | (12,407 | ) | (12.1 | ) | ||||||||||||||||
Interest income | 83 | 0.1 | 197 | 0.4 | 168 | 0.1 | 498 | 0.5 | ||||||||||||||||||||
Interest expense | (11 | ) | — | (1 | ) | — | (18 | ) | — | (3 | ) | — | ||||||||||||||||
Exchange rate (loss) gain | (423 | ) | (0.6 | ) | 871 | 1.6 | (544 | ) | (0.4 | ) | (257 | ) | (0.2 | ) | ||||||||||||||
Other, net | (9 | ) | — | — | — | (19 | ) | — | — | — | ||||||||||||||||||
Income (loss) before provision for income taxes | 5,669 | 7.7 | (4,749 | ) | (8.7 | ) | 2,008 | 1.4 | (12,169 | ) | (11.8 | ) | ||||||||||||||||
Provision for income taxes | 253 | 0.3 | 518 | 1.0 | 628 | 0.4 | 712 | 0.7 | ||||||||||||||||||||
Net income (loss) | $ | 5,416 | 7.4 | % | $ | (5,267 | ) | (9.7 | )% | $ | 1,380 | 1.0 | % | $ | (12,881 | ) | (12.5 | )% | ||||||||||
The following table sets forth our revenues by product expressed as dollar amounts (in thousands) and the changes in revenues between the specified periods expressed as percentages:
Three Months Ended June 30, | Percentage Change | Six Months Ended June 30, | Percentage Change | |||||||||||||||
2010 | 2009 | 2009 to 2010 | 2010 | 2009 | 2009 to 2010 | |||||||||||||
Medical segment: | ||||||||||||||||||
Consoles | $ | 10,796 | $ | 9,317 | 15.9 | % | $ | 19,456 | $ | 17,813 | 9.2 | % | ||||||
Single-procedure disposables: | ||||||||||||||||||
IVUS | 40,931 | 31,808 | 28.7 | 79,481 | 60,352 | 31.7 | ||||||||||||
FM | 10,752 | 7,209 | 49.1 | 21,304 | 13,469 | 58.2 | ||||||||||||
Other | 4,317 | 2,089 | 106.7 | 7,995 | 4,370 | 83.0 | ||||||||||||
Sub-total medical segment | 66,796 | 50,423 | 32.5 | 128,236 | 96,004 | 33.6 | ||||||||||||
Industrial segment | 6,656 | 3,619 | 83.9 | 11,788 | 6,997 | 68.5 | ||||||||||||
$ | 73,452 | $ | 54,042 | 35.9 | $ | 140,024 | $ | 103,001 | 35.9 | |||||||||
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The following table sets forth our revenues by geography expressed as dollar amounts (in thousands) and the changes in revenues in the specified periods expressed as percentages:
Three Months Ended June 30, | Percentage Change | Six Months Ended June 30, | Percentage Change | |||||||||||||||
2010 | 2009 | 2009 to 2010 | 2010 | 2009 | 2009 to 2010 | |||||||||||||
Revenues (1): | ||||||||||||||||||
United States | $ | 33,948 | $ | 26,641 | 27.4 | % | $ | 62,904 | $ | 50,851 | 23.7 | % | ||||||
Japan | 18,623 | 11,776 | 58.1 | 36,720 | 23,460 | 56.5 | ||||||||||||
Europe, the Middle East and Africa | 15,016 | 11,738 | 27.9 | 29,123 | 21,374 | 36.3 | ||||||||||||
Rest of world | 5,865 | 3,887 | 50.9 | 11,277 | 7,316 | 54.1 | ||||||||||||
$ | 73,452 | $ | 54,042 | 35.9 | $ | 140,024 | $ | 103,001 | 35.9 | |||||||||
(1) | Revenues are attributed to geographies based on the location of the customer, except for shipments by original equipment manufacturers, which are attributed to the country of the origin of the equipment distributed. |
Comparison of Three Months Ended June 30, 2010 and 2009
Revenues. Revenues increased $19.4 million, or 35.9%, to $73.5 million in the three months ended June 30, 2010, as compared to revenues of $54.0 million in the three months ended June 30, 2009. In the three months ended June 30, 2010, revenues related to IVUS single-procedure disposables increased $9.1 million, or 28.7%, as compared to the three months ended June 30, 2009. Revenues related to console sales in the three months ended June 2010 increased $1.5 million, or 15.9%, primarily resulting from increased console sales. Overall, our revenue increases were driven by increased demand for our disposables, as well as higher revenues resulting from our direct sales efforts in Japan. Additionally, the increases in FM disposable revenues were primarily due to the broader availability of FFR technology as this functionality has been incorporated into our multi-modality console, in conjunction with an increased adoption of the technology based on clinical study data. Industrial segment revenues were $6.7 million in the three months ended June 30, 2010 as compared to $3.6 million in the same period last year, resulting from higher sales to our international telecommunications customers. Other revenues increased $2.2 million, primarily due to higher sales of third party products and higher service contract and rental revenues. Increases in revenues were realized across all our key geographic markets.
Cost of Revenues. Cost of revenues increased $4.6 million, or 20.5%, to $27.1 million, or 36.9% of revenues in the three months ended June 30, 2010, from $22.5 million, or 41.6% of revenues in the three months ended June 30, 2009. The increase in the cost of revenues was primarily due to higher sales volume. Gross margin was 63.1% of revenues in the three months ended June 30, 2010, increasing from 58.4% of revenues in the three months ended June 30, 2009. This favorable gross margin was primarily the result of increased overhead recovery rates due to higher volumes, favorable pricing impact from our transition to the direct sales model in Japan, as well as a decrease in the production costs of IVUS and FM disposable products due to ongoing cost reduction initiatives and lower warranty related costs.
Selling, General and Administrative. Selling, general and administrative expenses increased $3.6 million, or 13.7%, to $30.1 million, or 41.0% of revenues in the three months ended June 30, 2010, as compared to $26.5 million, or 48.9% of revenues in the three months ended June 30, 2009. The increase in the three months ended June 30, 2010 as compared with the three months ended June 30, 2009 was primarily due to continued growth in our Japan operation to support our direct sales efforts there, legal expenses related to the LightLab litigation and increased headcount resulting from the expansion of our U.S. and Europe sales organizations.
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Research and Development. Research and development expenses decreased $272,000, or 2.8%, to $9.6 million, or 13.1% of revenues in the three months ended June 30, 2010, as compared to $9.9 million, or 18.3% of revenues in the three months ended June 30, 2009. The decrease in research and development expenses in the three months ended June 30, 2010 as compared with the three months ended June 30, 2009 was primarily due to the timing of spending on various product development projects.
In-process research and development.We recorded $33,000 of IPR&D expenses in the three months ended June 30, 2010 related to the milestone achieved under the OCT program. There were no IPR&D expenses in the three months ended June 30, 2009.
Amortization of Intangibles. Amortization expense decreased to $621,000, or 0.8% of revenues in the three months ended June 30, 2010, as compared to $1.1 million, or 1.9% of revenues in the three months ended June 30, 2009. The decrease is primarily related to developed technology that we originally acquired from Jomed, NV that was fully amortized as of December 2009.
Interest Income. Interest income decreased to $83,000, or 0.1% of revenues in the three months ended June 30, 2010, as compared to $197,000, or 0.4% of revenues in the three months ended June 30, 2009. The decrease was primarily due to a decrease in the weighted-average interest rate earned on our investments.
Exchange Rate (Loss) Gain. Exchange rate loss for the three months ended June 30, 2010 was $423,000, as compared to an exchange rate gain of $871,000 in the three months ended June 30, 2009. The exchange rate loss for the three months ended June 30, 2010, primarily related to the strengthening of the U.S. dollar against the euro and its impact on our intercompany receivable balances. The exchange rate gain for the three months ended June 30, 2009 primarily related to the weakening U.S. dollar compared to the yen and the related effect on the valuation of yen based monetary assets and liabilities held by Volcano Japan. In October 2009, approximately $23.4 million of intercompany receivable amounts owed to Volcano Corporation from Volcano Japan were converted to long-term investment, resulting in a decrease in the amount of yen-based receivables being marked to market. In addition, during the three months ended June 30, 2010, we mitigated the effects of exchange rate changes to our intercompany receivable balances through our hedging practices.
Provision for Income Taxes. Provision for income taxes for the three months ended June 30, 2010 was $253,000, compared to a provision of $518,000 for the three months ended June 30, 2009. Stock option excess tax benefits of $176,000 were credited to additional paid-in-capital through June 30, 2010.
Comparison of Six Months Ended June 30, 2010 and 2009
Revenues. Revenues increased $37.0 million, or 35.9%, to $140.0 million in the six months ended June 30, 2010, as compared to revenues of $103.0 million in the six months ended June 30, 2009. In the six months ended June 30, 2010, revenues related to IVUS single-procedure disposables increased $19.1 million, or 31.7%, as compared to the six months ended June 30, 2009. Revenues related to console sales in the six months ended June 2010 increased 9.2% as compared to the same period last year, based on an increase in console unit sales. Overall, our revenue increases were driven by increased demand for our disposables, as well as higher revenues resulting from our direct sales efforts in Japan. Additionally, the increases in FM disposable revenues were primarily due to the broader availability of FFR technology as this functionality has been incorporated into our multi-modality console, in conjunction with an increased adoption of the technology based on clinical study data. Industrial segment revenues were $11.8 million in the six months ended June 30, 2010 as compared to $7.0 million in the same period last year, resulting from higher sales to our international telecommunications customers. Other revenues increased $3.6 million, primarily due to higher sales of third party products and higher service contract and rental revenues. Increases in revenues were realized across all our key geographic markets.
Cost of Revenues. Cost of revenues increased $10.6 million, or 24.6%, to $53.7 million, or 38.4% of revenues in the six months ended June 30, 2010, from $43.1 million, or 41.9% of revenues in the six months ended June 30, 2009. The increase in the cost of revenues was primarily due to higher sales volume. Gross margin was 61.6% of revenues in the six months ended June 30, 2010, increasing from 58.1% of revenues in the six months ended June 30, 2009. This favorable gross margin was primarily the result of favorable pricing on our IVUS and FM disposable products, favorable pricing impact from our transition to the direct sales model in Japan, and a decrease in the production costs of IVUS and FM disposable products due to ongoing cost reduction initiatives and lower warranty related costs.
Selling, General and Administrative. Selling, general and administrative expenses increased $11.6 million, or 22.6%, to $63.2 million, or 45.1% of revenues in the six months ended June 30, 2010, as compared to $51.5 million, or 50.0% of revenues in the six months ended June 30, 2009. The increase in the six months ended June 30, 2010 as compared with the six months ended June 30, 2009 was primarily due to continued growth in our Japan operation to support our direct sales efforts there, legal expenses related to the LightLab litigation, increased headcount resulting from the expansion of our U.S. and Europe sales organizations, increased infrastructure expenses to support company growth, higher stock-based compensation expense, severance payments related to the resignation of two senior executives, and restructuring costs for the closure of our San Antonio facility.
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Research and Development. Research and development expenses increased $817,000, or 4.4%, to $19.5 million, or 13.9% of revenues in the six months ended June 30, 2010, as compared to $18.6 million, or 18.1% of revenues in the six months ended June 30, 2009. The increase in research and development expenses in the six months ended June 30, 2010 as compared with the six months ended June 30, 2009 was primarily due to increased spending on various product development projects and increased clinical and regulatory expenses.
In-process research and development.We recorded $65,000 of IPR&D expenses in the six months ended June 30, 2010 related to the milestone achieved under the OCT program. There were no IPR&D expenses in the six months ended June 30, 2009.
Amortization of Intangibles. Amortization expense decreased to $1.2 million, or 0.9% of revenues in the six months ended June 30, 2010, as compared to $2.1 million, or 2.0% of revenues in the six months ended June 30, 2009. The decrease is primarily related to developed technology that we originally acquired from Jomed, NV that was fully amortized as of December 2009.
Interest Income. Interest income decreased to $168,000, or 0.1% of revenues in the six months ended June 30, 2010, as compared to $498,000, or 0.5% of revenues in the six months ended June 30, 2009. The decrease was primarily due to a decrease in the weighted-average interest rate earned on our investments.
Exchange Rate Loss. Exchange rate loss for the six months ended June 30, 2010 was $544,000, as compared to a loss of $257,000 in the six months ended June 30, 2009. The exchange rate loss for the six months ended June 30, 2010 primarily related to the strengthening of the U.S. dollar against the euro and its impact on our intercompany receivable balances, while the loss in the six months ended June 30, 2009 primarily related to the strengthening of the U.S. dollar compared to the yen and the related effect on the valuation of yen based monetary assets and liabilities held by Volcano Japan.
Provision for Income Taxes. Provision for income taxes for the six months ended June 30, 2010 was $628,000, compared to a provision of $712,000 for the six months ended June 30, 2009. Stock option excess tax benefits of $176,000 were credited to additional paid-in-capital through June 30, 2010.
Liquidity and Capital Resources
Sources of Liquidity
Historically, our sources of cash have included:
• | issuance of equity securities, including underwritten public offerings of our common stock, cash generated from the exercise of stock options and participation in our employee stock purchase plan; |
• | cash generated from operations, primarily from the collection of accounts receivable resulting from product sales; and |
• | interest income. |
Our historical cash outflows have primarily been associated with:
• | cash used for operating activities such as the purchase and growth of inventory, expansion of our sales and marketing and research and development infrastructure and other working capital needs; |
• | expenditures related to increasing our manufacturing capacity and improving our manufacturing efficiency; |
• | capital expenditures related to the acquisition of equipment that we own and place at our customer premises and other fixed assets; |
• | cash used to repay our debt obligations and related interest expense; and |
• | cash used for acquisitions. |
Fluctuations in our working capital due to timing differences of our cash receipts and cash disbursements also impact our cash inflow and outflow.
At June 30, 2010, our cash and cash equivalents and available-for-sale investments totaled $131.4 million. We invest our excess funds primarily in short-term securities issued by corporations, banks, the U.S. government, municipalities, financial holding companies and in money market funds comprised of U.S. Treasury and agency securities. We do not hold securities backed by mortgages.
At June 30, 2010, our accumulated deficit was $131.9 million. Since inception, we have generated significant operating losses and as a result we have not generated sufficient cash flow to fund our operations and the growth in our business. Accordingly, prior to our initial public offering, we financed our operations and acquisitions primarily through the issuances of $62.5 million of preferred stock, $20.0 million of senior subordinated notes and $7.0 million of term loans. These issuances of equity and debt were supplemented with borrowings from a revolving credit facility and equipment financing arrangements. The issuances of our senior subordinated notes, term loans and revolving credit facility included warrants to purchase our common stock or Series B preferred stock, which automatically converted into warrants to purchase common stock upon the completion of our initial public offering.
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Cash Flows
Cash Flows from Operating Activities. Cash provided by operating activities of $10.5 million for the six months ended June 30, 2010 reflected our net income of $1.4 million, increased by adjustments for non-cash expenses, consisting primarily of $8.8 million of depreciation and amortization, and $6.2 million of stock-based compensation expense. The change was also impacted by changes in working capital items, including increases in accounts receivable of $1.7 million due to increased sales, increased inventories of $1.5 million, decreases in accrued expenses and other liabilities of $2.1 million, and a decrease in accrued compensation of $907,000.
Cash Flows from Investing Activities. Cash used by investing activities was $25.6 million in the six months ended June 30, 2010, consisting primarily of $48.7 million used to purchase short-term available-for-sale investments, $8.4 million used for capital expenditures, as well as $2.1 million used for acquisition of intangible assets, $1.1 million payments for foreign currency exchange forward contracts, and $596,000 cash paid related to milestone payments, partially offset by $33.9 million resulting from the sale or maturity of short-term available-for-sale investments and $1.4 million proceeds from foreign currency exchange contracts.
Cash Flows from Financing Activities. Cash provided by financing activities was $8.4 million in the six months ended June 30, 2010, resulting primarily from proceeds of $7.1 million from the exercise of common stock options and $1.2 million from the issuance of stock under our employee stock purchase plan. While we are not able to predict cash proceeds from future stock option exercises, we do not anticipate similar proceeds for the remainder of the year.
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Future Liquidity Needs
At June 30, 2010, we believe our current cash and cash equivalents and our short-term available-for-sale investments will be sufficient to fund working capital requirements, capital expenditures, and operations for at least the next twelve months. We intend to retain any future earnings to support operations and to finance the growth and development of our business, and we do not anticipate paying any dividends in the foreseeable future. At the present time, we have no material commitments for capital expenditures.
Our future liquidity and capital requirements will be influenced by numerous factors, including the extent and duration of future operating losses, the level and timing of future sales and expenditures, the results and scope of ongoing research and product development programs, working capital required to support our sales growth, the receipt of and time required to obtain regulatory clearances and approvals, our sales and marketing programs, the continuing acceptance of our products in the marketplace, competing technologies, changes in the market and regulatory environment and cash that may be required to settle our foreign currency hedges.
Our ability to fund our longer-term cash needs is subject to various risks, many of which are beyond our control—See Part II, Item 1A—”Risk Factors” set forth in this document and our annual report on Form 10-K for the fiscal year ended December 31, 2009. Should we require additional funding, such as additional capital investments, we may need to raise the required additional funds through bank borrowings or public or private sales of debt or equity securities. We cannot assure that such funding will be available in needed quantities or on terms favorable to us, if at all.
Critical Accounting Policies
The discussion and analysis of our financial condition and results of operations are based upon our unaudited condensed consolidated financial statements, which have been prepared in accordance with U.S. generally accepted accounting principles. The preparation of these financial statements requires us to make estimates and judgments that affect the reported amounts of assets, liabilities, revenues and expenses. On an on-going basis, we evaluate our critical accounting policies and estimates. We base our estimates on historical experience and on various other assumptions that we believe to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Actual results may differ from these estimates under different assumptions or conditions. Our critical accounting policies and estimates are discussed in our annual report on Form 10-K for the fiscal year ended December 31, 2009.
In October 2009, the Financial Accounting Standards Board, or FASB, issued Accounting Standards Update, or ASU, No. 2009-13,Revenue Recognition (Topic 605): Multiple-Deliverable Revenue Arrangements,or ASU 2009-13, and ASU No. 2009-14,Software (Topic 985): Certain Revenue Arrangements That Include Software Elements,or ASU 2009-14. ASU 2009-13 provides for two significant changes to the existing multiple-element revenue arrangements guidance. The first relates to the determination of when the individual deliverables included in a multiple-element arrangement may be treated as separate units of accounting. This change is significant as it will likely result in the requirement to separate more deliverables within an arrangement, ultimately leading to less revenue deferral. The second change modifies the manner in which the transaction consideration is allocated across the separately identified deliverables. ASU 2009-14 updates guidance on how entities account for revenue arrangements that contain both hardware and software elements.
We prospectively adopted ASU 2009-13 and ASU 2009-14 on January 1, 2010. We have applied ASU 2009-13 to our revenue arrangements containing multiple deliverables that were entered into or significantly modified on or after January 1, 2010. These deliverables can consist of consoles, options for the console, single-procedure disposable products, service and maintenance agreements, biomedical equipment education and exchange rights for alternative platforms of our product functionality. As a result of adopting ASU 2009-13, we have identified additional separate units of accounting related to options for our consoles, biomedical equipment education and exchange rights for alternative platforms of our product functionality. We allocate arrangement consideration based on the relative selling prices of the separate units of accounting contained within an arrangement containing multiple deliverables. Selling prices are determined using fair value, when available, or our estimate of selling price when fair value is not available for a given unit of accounting. Significant inputs in our estimates of the selling price of separate units of accounting include market and pricing trends, a customer’s geographic location and the expected gross margins by product line. Prior to the adoption of ASU 2009-13, we used the residual method to allocate the arrangement consideration when we had not established fair value of delivered items and deferred all arrangement consideration when fair value was not available for undelivered items. Typically, we complete all obligations under an arrangement with multiple deliverables within one year.
The adoption of ASU 2009-13 did not have a material impact on our consolidated financial position or results of operations as of and for the three and six month periods ending June 30, 2010. As a result of adopting ASU 2009-13, we recognized additional revenues in the three and six months ended June 30, 2010 of $468,000 and $745,000, respectively. Had we adopted ASU 2009-13 on January 1, 2009, we would have recognized additional revenues in the three and six months ended June 30, 2009 of $193,000 and $381,000, respectively.
The adoption of ASU 2009-14 did not impact our consolidated financial position or results of operations.
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Other than the adoption of the revenue recognition guidance detailed above, there have been no other material changes to our accounting policies during the six months ended June 30, 2010.
Off-Balance Sheet Arrangements
At June 30, 2010, we did not have any off-balance sheet arrangements that have or are reasonably likely to have a current or future material effect on our financial condition, changes in financial condition, revenues or expenses, results of operations, liquidity, capital expenditures or capital resources.
Contractual Obligations
In addition to the contractual obligations disclosed in Part II, Item 7 of our annual report on Form 10-K for the year ended December 31, 2009, in January 2010 we entered into a lease agreement for approximately 32,000 square feet of office space for our corporate headquarters in San Diego, California for which we are obligated to pay approximately $5.2 million of rent over a five year period commencing on August 1, 2010. The lease contains a rent escalation clause of approximately 3% per year in each of the successive years of the lease term. We also have the option to renew the lease for an additional three year period.
Item 3. | Quantitative and Qualitative Disclosures About Market Risk |
Market risk represents the risk of changes in the value of market risk sensitive instruments caused by fluctuations in interest rates, foreign exchange rates and commodity prices. Changes in these factors could cause fluctuations in our results of operations and cash flows.
Our exposure to interest rate risk at June 30, 2010 is related to the investment of our excess cash into highly liquid, short-term financial investments. We invest in cash and cash equivalents and short-term available-for-sale investments in accordance with our investment policy. The primary objectives of our investment policy are to preserve principal, maintain proper liquidity to meet operating needs and obtain the best yields available consistent with the investment risk. Our investment policy specifies credit quality standards for our investments. We do not hold mortgage-backed securities. Due to the short-term nature of the majority of our investments, we have assessed that there is no material exposure to interest rate risk arising from them.
We are exposed to foreign currency risk related to our European and Japanese operations. Fluctuations in the rate of exchange between the U.S. dollar and foreign currencies, primarily the euro and the yen, could adversely affect our financial results. During the six months ended June 30, 2010, our revenues were unfavorably impacted by the valuation of the euro and favorably impacted by the valuation of the yen, as compared to the U.S. dollar. In periods of a strengthening U.S. dollar, our results of operations including the amount of revenue that we report in future periods could be negatively impacted. Commencing October 2009, we began using foreign exchange forward contracts to manage a portion of the foreign currency exposure risk for our monetary assets and liabilities denominated in the yen and the euro. We only use derivative instruments to reduce foreign currency exchange rate risks; we do not hold any derivative financial instruments for trading or speculative purposes. We primarily use foreign exchange forward contracts to hedge foreign currency exposures, and they generally have terms of one year or less. Realized and unrealized gains or losses on the value of financial contracts used to hedge the exchange rate exposure of these monetary assets and liabilities are also included in the determination of net income, as these transactions have not been designated for hedge accounting. These contracts effectively fix the exchange rate at which these specific monetary assets and liabilities will be settled so that gains or losses on the forward contracts offset the gains or losses from changes in the value of the underlying monetary assets and liabilities. These contracts contain net settlement features. If we experience unfavorable changes in foreign exchange rates, we may be required to use material amounts of cash to settle the transactions which may adversely affect the operating results that we report with respect to the corresponding period.
We currently hold foreign exchange forward contracts with a single counterparty. The bank counterparty in these contracts exposes us to credit-related losses in the event of their nonperformance. However, to mitigate that risk, we only contract with counterparties who meet our minimum credit quality guidelines. In addition, our exposure in the event of a default by our counterparty is limited to the changes in value of our hedged balances.
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Item 4. | Controls and Procedures |
Evaluation of disclosure controls and procedures
Under the supervision and with the participation of our management, including our chief executive officer and our chief financial officer, we carried out an evaluation of the effectiveness of the design and operation of our disclosure controls and procedures as defined in Rules 13a-15(e) and 15d-15(e) under the Securities Exchange Act of 1934, as amended, or the Exchange Act. Based on that evaluation, our chief executive officer and our chief financial officer have concluded that, at June 30, 2010, our disclosure controls and procedures were effective.
Disclosure controls and procedures are controls and other procedures that are designed to ensure that information required to be disclosed in our reports filed or submitted under the Exchange Act is recorded, processed, summarized and reported within the time periods specified in the SEC’s rules and forms. Disclosure controls and procedures include, without limitation, controls and procedures designed to ensure that information required to be disclosed in our reports filed under the Exchange Act is accumulated and communicated to our management, including our chief executive officer and chief financial officer, or persons performing similar functions, as appropriate, to allow timely decisions regarding required disclosure.
Changes in internal control over financial reporting
Under the supervision and with the participation of our management, including our chief executive officer and our chief financial officer, we carried out an evaluation of any potential changes in our internal control over financial reporting during the fiscal quarter covered by this quarterly report on Form 10-Q.
There were no changes in our internal control over financial reporting during the quarter ended June 30, 2010 that our certifying officers concluded materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.
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Item 1. | Legal Proceedings |
The information set forth under Note 4—”Commitments and Contingencies– Litigation” of our Notes to Unaudited Consolidated Financial Statements, included in Part I, Item 1 of this quarterly report, is incorporated herein by reference.
Item 1A. | Risk Factors |
This “Risk Factors” section provides updated information in certain areas from the “Risk Factors” set forth in our annual report on Form 10-K for the fiscal year ended December 31, 2009, or the Annual Report. Set forth below are certain risk factors that have been updated from the Annual Report. The risks and uncertainties described in the Annual Report, as added, expanded or updated below do not constitute all the risk factors that pertain to our business but we do believe that they reflect the more important ones. Please review the Annual Report for a complete listing of “Risk Factors” that pertain to our business.
Risks Related to Our Business and Industry
We have a limited operating history, have incurred significant operating losses since inception and cannot assure you that we will sustain profitability.
We were formed in January 2000 and until 2003 were a development stage company substantially devoted to the research and development of tools designed to diagnose vulnerable plaque. In July 2003, we acquired substantially all of the assets related to the IVUS and FM product lines from Jomed, Inc. and commenced the manufacturing, sale and distribution of IVUS and FM products. We have yet to generate sufficient revenues to sustain profitability. Even if we do increase revenues, we expect our operating expenses will increase as we expand our business to meet anticipated growing demand for our products and as we devote resources to our sales, marketing and research and development activities. If we are unable to reduce our cost of revenues and our operating expenses, we may not achieve sustained profitability. Although we achieved profitability during the quarters ended June 30, 2010, December 31, 2008 and September 30, 2008, you should not rely on our operating results for any prior quarterly or annual period as an indication of our future operating performance. At June 30, 2010, we had an accumulated deficit of $131.9 million. We expect to experience quarterly fluctuations in our revenues due to the timing of capital purchases by our customers and to a lesser degree the seasonality of disposable consumption by our customers. Additionally, expenses will fluctuate as we make future investments in research and development, selling and marketing and general and administrative activities. This will cause us to experience variability in our reported earnings and losses in future periods. Failure to achieve and sustain profitability would negatively impact the market price of our common stock.
The risks inherent in our international operations may adversely impact our revenues, results of operations and financial condition.
We derive, and anticipate we will continue to derive, a significant portion of our revenues from operations in Japan and Europe. In the six months ended June 30, 2010, revenues to customers located in Japan were $36.7 million and Europe, Middle East and Africa were $29.1 million, representing approximately 26% and 21%, respectively, of our total revenues. As we expand internationally, we will need to hire, train and retain qualified personnel for our direct sales efforts, retain distributors and train their personnel in countries where language, cultural or regulatory impediments may exist. We cannot ensure that distributors, physicians, regulators or other government agencies will accept our products, services and business practices. In addition, we purchase some components on the international market. The sale and shipment of our products and services across international borders, as well as the purchase of components from international sources, subject us to extensive U.S. and foreign governmental trade regulations. Compliance with such regulations is costly. Any failure to comply with applicable legal and regulatory obligations could impact us in a variety of ways that include, but are not limited to, significant criminal, civil and administrative penalties, including imprisonment of individuals, fines and penalties, denial of export privileges, seizure of shipments and restrictions on certain business activities. Failure to comply with applicable legal and regulatory obligations could result in the disruption of our shipping and sales activities. Our international sales operations expose us and our representatives, agents and distributors to risks inherent in operating in foreign jurisdictions, including:
• | our ability to obtain, and the costs associated with obtaining, United States export licenses and other required export or import licenses or approvals; |
• | changes in duties and tariffs, taxes, trade restrictions, license obligations and other non-tariff barriers to trade; |
• | burdens of complying with a wide variety of foreign laws and regulations related to healthcare products; |
• | costs of localizing product and service offerings for foreign markets; |
• | business practices favoring local companies; |
• | longer payment cycles and difficulties collecting receivables through foreign legal systems; |
• | difficulties in enforcing or defending agreements and intellectual property rights; and |
• | changes in foreign political or economic conditions. |
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We cannot ensure that one or more of these factors will not harm our business. Any material decrease in our international revenues or inability to expand our international operations would adversely impact our revenues, results of operations and financial condition.
Fluctuations in foreign currency exchange rates could result in declines in our reported revenues and earnings.
Our reported revenues and earnings are subject to fluctuations in currency exchange rates. Prior to October 2009 we did not engage in hedging activities with respect to our foreign currency exchange risk. Commencing October 2009, we began using foreign exchange forward contracts to manage a portion of the foreign currency exposure risk for foreign subsidiaries with monetary assets and liabilities denominated in the yen and the euro. We do not engage in foreign currency hedging arrangements for our revenues or operating expenses, and, consequently, foreign currency fluctuations may adversely affect our revenues and earnings. We cannot be assured our hedges will be effective or that the costs of the hedges will not exceed their benefits. Fluctuations in the rate of exchange between the U.S. dollar and foreign currencies, primarily the euro and the yen, could require material amounts of cash to settle the hedge transactions or adversely affect our financial results. During the six months ended June 30, 2010, 16.6% and 26.2% of our revenues were denominated in the euro and yen, respectively, 10.2% of our operating expenses were denominated in the euro and 12.9% of our operating expenses were denominated in the yen. Historically, revenues from our Japanese operations were primarily denominated in the U.S. dollar. Due to recent and expected increases in direct sales denominated in the Japanese yen as well as the integration of our Japan operations into the local economic environment, effective July 1, 2009, we changed the functional currency of Volcano Japan to the Japanese yen. During the six months ended June 30, 2010, the U.S. dollar strengthened versus the yen. In periods of a strengthening U.S. dollar relative to the yen, our results of operations that we report in future periods could be negatively impacted.
We are subject to federal, state and foreign healthcare laws and regulations and implementation or changes to such healthcare laws and regulations could adversely affect our business and results of operations.
In an effort to contain rising healthcare costs, the U.S. federal government recently enacted comprehensive health care reform legislation, which may significantly affect the payment for, and the availability of, healthcare services and result in fundamental changes to federal healthcare reimbursement programs. We are unable to predict at this time the impact of such recently enacted federal healthcare reform legislation on the medical device industry in general, or on us in particular and what, if any, additional legislation or regulation relating to the medical device industry may be enacted in the future. An expansion in the government’s role in the U.S. healthcare industry may lower reimbursements for procedures using our products, reduce medical procedure volumes and adversely affect our business and results of operations. Although we cannot predict the many ways that the federal healthcare reform legislation might affect our business, the federal healthcare reform legislation imposes a 2.3% excise tax on certain transactions, including many U.S. sales of medical devices, which we expect will include U.S. sales of our products. This tax is scheduled to take effect in 2013. It is unclear whether and to what extent, if at all, other anticipated developments resulting from the federal healthcare reform legislation, such as an increase in the number of people with health insurance and an increased focus on preventive medicine, may provide us additional revenue to offset this increased tax. If additional revenue does not materialize, or if our efforts to offset the excise tax through spending cuts or other actions are unsuccessful, the increased tax burden would adversely affect our financial performance, which in turn could cause the price of our stock to decline. In addition, a number of foreign governments are also considering or have adopted proposals to reform their healthcare systems. Because a significant portion of our revenues from our operations is derived internationally, if significant reforms are made to the healthcare systems in other jurisdictions, our sales and results of operations may be materially and adversely impacted.
Our efforts to continue our transition to a direct sales force in Japan may not be successful or may cause us to incur additional expenses and reduced revenues sooner than initially planned. If we are not successful or incur such additional expenses sooner than expected, then our business and results of operations may be materially and adversely affected.
A significant portion of our annual revenues was derived from sales to our Japanese distributors, primarily Goodman Company, Ltd. (“Goodman”) (until we terminated our relationship, as described below), Fukuda Denshi Co., Ltd. and Johnson & Johnson K.K., Cordis Division. In the six months ended June 30, 2010, we generated revenues of $9.4 million, which accounted for approximately 6.7% of our revenues, from sales to our Japanese distributors. Sales to Japanese distributors accounted for 24.3% and 11.8% of our revenues in 2008 and 2009, respectively.
On July 8, 2009, we entered into a Distributor Termination Agreement with Goodman that terminated certain agreements between us and Goodman effective August 31, 2009 and provided for the transition of the distribution, formerly handled by Goodman, of Volcano products in Japan to Volcano Japan.
As we continue to transition to a direct sales force in Japan, we may terminate additional relationships with key distributors. There is no assurance that we will be successful in completing our transition to a direct sales force in Japan and that we will be able to continue to successfully place, sell and service our products in Japan through a direct sales force or to successfully insure the growth of our direct sales force that may be needed in the event we terminate additional distributor relationships. Our challenges and potential risks in connection with expanding our direct sales force in Japan include, but are not limited to, (a) the successful retention and servicing of current distributors and customers in Japan, (b) strong market adoption of our technology in Japan, (c) the achievement of our growth and market development strategies in Japan, and (d) our ability to recruit, train and retain an expanded direct sales force in Japan. In addition, to the extent we terminate additional relationships with distributors, we may incur significant additional expenses and reduced revenues sooner than initially planned. Our efforts to successfully expand our direct sales strategy in Japan or the failure to achieve our sales objectives in Japan may adversely impact our revenues, results of operations and financial condition and negatively impact our ability to sustain and grow our business in Japan.
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General national and worldwide economic conditions may materially and adversely affect our financial performance and results of operations.
Our operations and performance depend significantly on national and worldwide economic conditions and the resulting impact on purchasing decisions and the level of spending on our products by customers in the geographic markets in which our IVUS and FM products are sold or distributed. These economic conditions remain depressed significantly in many countries and regions, including without limitation the U.S., Japan, Europe, Middle East and Africa, where we have generated most of our revenues. If our customers do not obtain or do not have access to the necessary capital to operate their businesses, or are otherwise adversely affected by the deterioration in national and worldwide economic conditions, this could result in reductions in the sales of our products, longer sales cycles and slower adoption of new technologies by our customers, which would materially and adversely affect our business. In addition, our customers’, distributors’ and suppliers’ liquidity, capital resources and credit may be adversely affected by the availability of capital and credit crisis, which could adversely affect our ability to collect on our outstanding invoices and lengthen our collection cycles, distribute our products or limit our timely access to important sources of raw materials necessary for the manufacture of our consoles and catheters.
In addition, we have invested our excess cash in money market funds and corporate debt securities issued by banks and corporations. The interest paid on these types of investments and the value of certain securities may continue to decline as credit markets adjust to the national and global financial crisis. While our investment portfolio has experienced reduced yields, we have not yet experienced a deterioration of the credit quality of our holdings or other material adverse effects. If there is continued and expanded disruption in the credit markets, our investment portfolio could be adversely affected.
There can be no assurances that government responses to the disruptions in the financial or credit markets will improve the national and worldwide economic conditions in the near term or that the national and worldwide economic conditions will not worsen.
Item 6. | Exhibits |
Exhibit | Description of Exhibit | |
3.1 | Amended and Restated Certificate of Incorporation of the Registrant (filed as Exhibit 3.1 to the Registrant’s Quarterly Report on Form 10-Q (File No. 000-52045), as originally filed on August 9, 2006, and incorporated herein by reference). | |
3.2 | Bylaws of the Registrant (filed as Exhibit 3.1 to the Registrant’s Current Report on Form 8-K (File No. 000-52045), as originally filed on August 29, 2008, and incorporated herein by reference). | |
3.3 | Certificate of Designation of Series A Junior Participating Preferred Stock (filed as Exhibit 3.2 to the Registrant’s Quarterly Report on Form 10-Q (File No. 000-52045), as originally filed on August 9, 2006, and incorporated herein by reference). | |
4.1 | Reference is made to Exhibits 3.1, 3.2 and 3.3. | |
4.2 | Specimen Common Stock certificate of the Registrant (filed as Exhibit 4.1 to the Registrant’s Registration Statement on Form S-1/A, as amended (File No. 333-132678), as originally filed on May 24, 2006, and incorporated herein by reference). | |
4.3 | Fourth Amended and Restated Investor Rights Agreement, dated February 18, 2005, by and among the Registrant and certain stockholders (filed as Exhibit 4.2 to the Registrant’s Registration Statement on Form S-1, as amended (File No. 333-132678), as originally filed on March 24, 2006, and incorporated herein by reference). | |
4.4 | Rights Agreement, by and between the Registrant and American Stock Transfer & Trust Company, dated June 20, 2006 (filed as Exhibit 4.1 to the Registrant’s Quarterly Report on Form 10-Q (File No. 000-52045), as originally filed on August 9, 2006, and incorporated herein by reference). |
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Exhibit | Description of Exhibit | |
10.2 | Form of Restricted Stock Unit Grant Notice and Form of Restricted Stock Unit Agreement with deferred delivery under the Volcano Corporation 2005 Equity Compensation Plan, as amended and restated. | |
10.3 | Director Compensation Policy, as revised by the Registrant on May 5, 2010. | |
31.1 | Certification of the President & Chief Executive Officer pursuant to Rule 13a-14(a)/15d-14(a) of the Securities Exchange Act of 1934, as amended. | |
31.2 | Certification of the Chief Financial Officer pursuant to Rule 13a-14(a)/15d-14(a) of the Securities Exchange Act of 1934, as amended. | |
32.1* | Certification of the President & Chief Executive Officer pursuant to Rule 13a-14(b) or Rule 15d-14(b) of the Securities Exchange Act of 1934, as amended, and 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002. | |
32.2* | Certification of the Chief Financial Officer pursuant to Rule 13a-14(b) or Rule 15d-14(b) of the Securities Exchange Act of 1934, as amended, and 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002. |
* | The certifications attached as Exhibits 32.1 and 32.2 accompany this quarterly report on Form 10-Q pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, and shall not be deemed “filed” by the Registrant for purposes of Section 18 of the Securities Exchange Act of 1934, as amended. |
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Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.
Signature | Title | Date | ||
/S/ JOHN T. DAHLDORF John T. Dahldorf | Chief Financial Officer (principal financial officer, principal accounting officer and duly authorized officer) | August 5, 2010 |
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Exhibit Index
Exhibit | Description of Exhibit | |
3.1 | Amended and Restated Certificate of Incorporation of the Registrant (filed as Exhibit 3.1 to the Registrant’s Quarterly Report on Form 10-Q (File No. 000-52045), as originally filed on August 9, 2006, and incorporated herein by reference). | |
3.2 | Bylaws of the Registrant (filed as Exhibit 3.1 to the Registrant’s Current Report on Form 8-K (File No. 000-52045), as originally filed on August 29, 2008, and incorporated herein by reference). | |
3.3 | Certificate of Designation of Series A Junior Participating Preferred Stock (filed as Exhibit 3.2 to the Registrant’s Quarterly Report on Form 10-Q (File No. 000-52045), as originally filed on August 9, 2006, and incorporated herein by reference). | |
4.1 | Reference is made to Exhibits 3.1, 3.2 and 3.3. | |
4.2 | Specimen Common Stock certificate of the Registrant (filed as Exhibit 4.1 to the Registrant’s Registration Statement on Form S-1/A, as amended (File No. 333-132678), as originally filed on May 24, 2006, and incorporated herein by reference). | |
4.3 | Fourth Amended and Restated Investor Rights Agreement, dated February 18, 2005, by and among the Registrant and certain stockholders (filed as Exhibit 4.2 to the Registrant’s Registration Statement on Form S-1, as amended (File No. 333-132678), as originally filed on March 24, 2006, and incorporated herein by reference). | |
4.4 | Rights Agreement, by and between the Registrant and American Stock Transfer & Trust Company, dated June 20, 2006 (filed as Exhibit 4.1 to the Registrant’s Quarterly Report on Form 10-Q (File No. 000-52045), as originally filed on August 9, 2006, and incorporated herein by reference). | |
10.2 | Form of Restricted Stock Unit Grant Notice and Form of Restricted Stock Unit Agreement with deferred delivery under the Volcano Corporation 2005 Equity Compensation Plan, as amended and restated. | |
10.3 | Director Compensation Policy, as revised by the Registrant on May 5, 2010. | |
31.1 | Certification of the President & Chief Executive Officer pursuant to Rule 13a-14(a)/15d-14(a) of the Securities Exchange Act of 1934, as amended. | |
31.2 | Certification of the Chief Financial Officer pursuant to Rule 13a-14(a)/15d-14(a) of the Securities Exchange Act of 1934, as amended. | |
32.1* | Certification of the President & Chief Executive Officer pursuant to Rule 13a-14(b) or Rule 15d-14(b) of the Securities Exchange Act of 1934, as amended, and 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002. | |
32.2* | Certification of the Chief Financial Officer pursuant to Rule 13a-14(b) or Rule 15d-14(b) of the Securities Exchange Act of 1934, as amended, and 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002. |
* | The certifications attached as Exhibits 32.1 and 32.2 accompany this quarterly report on Form 10-Q pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, and shall not be deemed “filed” by the Registrant for purposes of Section 18 of the Securities Exchange Act of 1934, as amended. |
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