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U.S. Department of Health and Human Services

CDRH Advisory Meeting Materials Archive

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Name of CommitteeGeneral and Plastic Surgery Devices Panel
Date and TimeThe meeting was held on the following dates:
Nov 18, 08 8:30 AM - 5:00 PM
Nov 19, 08 8:00 AM - 12:30 PM
LocationMarriott Gaithersburg Washingtonian Center, Salons C and D
9751 Washingtonian Blvd.
Gaithersburg , MD
Contact InformationLisa M. Lim, Center for Devices and Radiological Health (HFZ–410), Food and Drug Administration, 9200 Corporate Blvd., Rockville, MD 20850, 240-276-3555, or FDA Advisory Committee Information Line, 1-800-741-8138 (301-443-0572 in the Washington, DC area), code 3014512519. 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.
AgendaOn November 18, 2008, the committee will receive an update on safety information collected on dermal fillers in the commercial setting, discuss current premarket and postmarket approved study designs, and make recommendations on general issues concerning the study of various dermal fillers. In addition, the committee will discuss the design of clinical trials for future premarket submissions seeking approval of dermal fillers for new intended uses. On November 19, 2008, the committee will discuss and make recommendations on general issues related to the clinical trials of cosmetic devices. Specifically, the committee will make recommendations on how to quantify the effects of devices with various types of energy sources, such as light-based products, light-based combination devices, ultrasound devices (including focused ultrasound devices), massagers combined with other energy modalities, cryogenic energy devices, radiofrequency ablation devices, and microwave systems, on dermatologic conditions. 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 2008 and scroll down to the appropriate advisory committee link.
ProcedureInterested 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 10, 2008. Oral presentations from the public will be scheduled between approximately 9 a.m. and 10 a.m., and between 1:15 p.m. and 2:15 p.m. on November 18, 2008, and between approximately 8:15 a.m. and 9:15 a.m. on November 19, 2008. 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 October 31, 2008. 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 3, 2008.
 Persons attending FDA’s advisory committee meetings are advised that the agency is not responsible for providing access to electrical outlets.
ConductFDA 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 (Nov 18)PDF
Agenda:Draft Agenda (Nov 19)PDF
Brief Summary:Summary of the November 18-19, 2008 Meeting - November 18, 2008Text
Brief Summary:Summary of the November 18-19, 2008 Meeting - November 19, 2008Text
Briefing:Briefing Information (Nov 19)Text
Briefing:Briefing Information (Nov 18)Text
Questions:Questions (Nov 18)PDF
Questions:Questions (Nov 19)PDF
Roster:Final Roster (Nov 19)PDF
Roster:Panel Roster (Nov 18)PDF
Slides:SlidesText
Transcript:November 18, Part 1PDF
Transcript:November 18, Part 3PDF
Transcript:November 19, Part 1PDF
Transcript:November 19, Part 2PDF
Transcript:November 18, Part 2PDF
Notice of this meeting is given under the Federal Advisory Committee Act (5 U.S.C. app. 2).
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