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| Name of Committee | Circulatory System Devices Panel |
| Date and Time | The meeting was held on the following dates:
Nov 29, 2007 8:00 AM - 6:00 PM
Nov 30, 2007 8:00 AM - 6:00 PM
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| Location | Gaithersburg Holiday Inn, Ballroom
2 Montgomery Village Ave.
Gaithersburg
, MD |
| Contact Information | James Swink, Center for Devices and Radiological Health (HFZ-450), Food and Drug Administration, 9200 Corporate Blvd., Rockville, MD 20850, 240-276-4179, or FDA Advisory Committee Information Line, 1-800-741-8138 (301-443-0572 in the Washington, DC area), code 3014512625. Please call the Information Line for up-to-date information on this meeting. A notice in the FEDERAL REGISTER about last minute modifications that impact a previously announced advisory committee meeting cannot always be published quickly enough to provide timely notice. Therefore, you should always check the agency’s Web site and call the appropriate advisory committee hot line/phone line to learn about possible modifications before coming to the meeting. |
| Agenda | On November 29, 2007, the committee will discuss, make recommendations, and vote on a premarket approval application, sponsored by Abbott Vascular, for the XIENCE™ V Everolimus Eluting Coronary Stent System, which is indicated for improving coronary luminal diameter in patients with symptomatic heart disease due to de novo native coronary artery lesions (length = 28 mm) with reference vessel diameter of 2.5 mm to 4.0 mm. On November 30, 2007, the committee will discuss, make recommendations, and vote on a premarket approval application, sponsored by Thoratec Corporation, for the HeartMate II Left Ventricular Assist System (LVAS), which is intended for use as a bridge to transplantation in cardiac transplant candidates at risk of imminent death from non-reversible left ventricular failure. The HeartMate II LVAS is intended for use both inside and outside the hospital. FDA intends to make background material available to the public no later than 2 business days before the meeting. If FDA is unable to post the background material on its Web site prior to the meeting, the background material will be made publicly available at the location of the advisory committee meeting, and the background material will be posted on FDA’s Web site after the meeting. Background material is available at http://www.fda.gov/ohrms/dockets/ac/acmenu.htm, click on the year 2007 and scroll down to the appropriate advisory committee link. |
| Procedure | Interested persons may present data, information, or views, orally or in writing, on issues pending before the committee. Written submissions may be made to the contact person on or before November 15, 2007. Oral presentations from the public will be scheduled for approximately 30 minutes at the beginning of committee deliberations on each day and for approximately 30 minutes near the end of the deliberations on each day. Those desiring to make formal oral presentations should notify the contact person and submit a brief statement of the general nature of the evidence or arguments they wish to present, the names and addresses of proposed participants, and an indication of the approximate time requested to make their presentation on or before November 7, 2007. Time allotted for each presentation may be limited. If the number of registrants requesting to speak is greater than can be reasonably accommodated during the scheduled open public hearing session, FDA may conduct a lottery to determine the speakers for the scheduled open public hearing session. The contact person will notify interested persons regarding their request to speak by November 8, 2007. |
| | Persons attending FDA’s advisory committee meetings are advised that the agency is not responsible for providing access to electrical outlets. |
| Conduct | FDA is committed to the orderly conduct of its advisory committee meetings. Please visit our Web site at http://www.fda.gov/oc/advisory/ for procedures on public conduct during advisory committee meetings. |
| Related Documents |
| Agenda: | Draft Agenda for November 29 |  |
| Brief Summary: | Summary from the Circulatory System Devices Panel Meeting - November 29, 2007 |  |
| Brief Summary: | Summary from the Circulatory System Devices Panel Meeting - November 30, 2007 | |
| Briefing: | Briefing Information for November 29 | |
| Other: | Waivers for Conflicts of Interest | |
| Questions: | Draft Questions for November 29 | |
| Roster: | Draft Public Roster for November 29 | |
| Slides: | Slides for November 29 and 30, 2007 Meeting | |
| Transcript: | Transcript for November 29, 2007 Meeting | |
| Transcript: | Transcript for November 29, 2007 Meeting | |
| Transcript: | Transcript for November 29, 2007 Meeting | |
| Transcript: | Transcript for November 29, 2007 Meeting | |
| Transcript: | Transcript for November 29, 2007 Meeting | |
| Transcript: | Transcript for November 30, 2007 Meeting | |
| Transcript: | Transcript for November 30, 2007 Meeting | |
| Transcript: | Transcript for November 30, 2007 Meeting | |
| Transcript: | Transcript for November 30, 2007 Meeting | |
| Transcript: | Transcript for November 30, 2007 Meeting | |
| Transcript: | Transcript for November 29, 2007 Meeting | |
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| Notice of this meeting is given under the Federal Advisory Committee Act (5 U.S.C. app. 2). |
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