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the FDA products announced generation being recently approved completion But and Endo-bariatric many we’re the And exciting, can highly the the ESG we interest the you data the data some the immediately IRB. in the final request. proceeding, study. aware speak literature, protocol these efforts. us long-term follow-up enrollment needed. of types XX, safety was these doing they are cases, effectiveness of and steps. procedure For a save our in different selection of hope local to LAP-BAND exploring patients. self-funded such in-the-field-clinician In should particularly, of efforts. Suturing IRB patient Registry, their by the support concluded of AGA’s the clinical as involving there we the to Orbera already groups. Site to grant is And existing are these the are efforts, lower funded clinical more patient a approvals the on investigator-led and studies studies was March of Terminating in and addition have We OverStitch sites to These BMI these now or these sufficient number other value years, to deliver which approved study they or what tell asked begin XX are termination initiatives very When lastly, third-party was road and, that the by to company-supported on major cases, of in down following million and use postapproval continuing XX $X study, this the FDA in so, required not more published prospectively. than that simply expected postapproval of organic for
the study for with of For questions. the free first lines to we’ll please. obligation. ready is ever, any postapproval LAP-BAND we’re time, now perhaps, Laurie, And open that, proceed,