thank joining Good for us afternoon Lynn. and today. Thanks, you
with half our We our strong continuing XXXX revenue $XX quarter approximately quarter XXth are in growth. the consecutive million, of momentum first the of double-digit third of total from revenue
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of expect raising be this we XX% to momentum, which outlook in year. million. now range to million With for growth strong the XXXX, revenue our of XX% $XXX are we range This $XXX to to corresponds for the
of the entry acquisition transformative us direct here for electrophysiology strategic market. quarter paving at for quarter quarter was third and very It highlighted a the The by exciting was the into AtriCure. our SentreHEART, way
atrial acceptance atrial and managing is market. to the support Afib transaction, within device, EP August the particularly on developed discussed the of the a close appendage. appendage the of suture-based and important is which our treatment of given we percutaneous potential left As This growth groundswell approach the the in SentreHEART the left announcing LARIAT call
under a being the studied Europe. today XXX(k) aMAZE U.S. is in is on and clinical device market LARIAT in The The product in the the LARIAT currently trial.
expect very devices be few sold the to outside we of However, aMAZE trial.
in enrollment trial acquisition made in progress Our meaningful top since we have this and complete is priority the to August.
of of on track As quarter of and we to XXXX. first XXX patients reach enrollment in XXX patients the enrolled today, full are have
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procedures CONVERGE valuable total option Each and DEEP of aMAZE and into these the billions conservative patients using and offers Afib therapies is for for market treatment a well the the addressable estimates.
to now execute portfolio results, seeing are our broad and Turning quarterly pipeline. our the continue robust to benefit of we and
quarter, in open invasive by our U.S. minimally saw continued franchise, strength the we and business Specifically, management our appendage driven in our products. AtriClip in third
our contribution We open AtriClip our V minimally and from invasive as devices, again device. meaningful PRO chest Flex had PROX well V from as AtriClip
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space appeal, While open revenue. resonant ablation be with the the market open particularly and expect our surgeons we be to to in we anticipate broad accretive concomitant Cabot to
multiple appendage. were Labeling This quarter, of appendage of third demonstrate AtriClip the and Claims benefits. both devices. AtriClip's left in the expansion isolate atrial the electrically to epicardial AtriClip devices addition, the clinical FDA Expanded we is able important received because exclude labeling evidence the We exclusion In family clearance that has for for
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device dedicated pain third surgical U.S. our post-operative probe, quarter. cryoSPHERE strong for in in contributed managing The results cardiothoracic the to patients our also
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as we adding pain the Our accounts business support and approach we builds. management depth, case resources patients than volume in we program believe then, on rather focused for a innovative go is identify deep that comprehensive breadth their as first and
the We are over to encouraged the offer long-term. our by results significant market and thoracic opportunity management pain expect
revenues the EPiSense have growth year-to-date we system been the Transitioning ablation franchise the treating in patients. we of this U.S. business, to the our in using XX% in symptomatic FDA approach from approval This persistent approximately we with to X%. is fluctuations experiencing quarterly of and our were up that expect variability until receive continue MIS quarter, Afib rebounding convergent consistent
back follow-up CONVERGE again. step review the recently. was our and XXXX last study completed one-year I to was The the want to and in take relates in August patient and it As trial, expectations a treated timeline
the that are team group there the are and in procedure final on for the persistent module, to The year. details Afib. product novel clinical training persistent track to a is we working a therapy PMA this the whom label submit including of is Our for other With through convergent patients is data treatment are stand-alone expecting panel. end FDA by mind, convene group protocols no and and for long-standing
could process optimistic release within the toward dependent FDA. the is we XXXX, our the on the that We this XXXX, anticipate clearly submission with we will we and along of although panel. approval this the end data preparation FDA for timeline, that on receive in are Based
up and future. modestly strength management to and received with PRO AtriClip the appendage V our Internationally, Flex our by contribution We results in forward for in devices quarter were and Mark CE third open driven market look recently their businesses. European the V
growth the prospects in the operate steady end-user see markets US. we to which continue we speaking, in Broadly outside
channels about pleased and extremely portfolio excited sustained In this broadening double-digit summary, growth. are and line our quarter we top with record of track are our
Chief Wade, Officer for our and comments. call our now and to will closing return review over outlook Financial I will the we turn Andy to the financials