The Food and Drug Administration (FDA) is announcing the following “CDRH Veteran Amputee Device Workshop.” The purpose of this workshop is to engage all stakeholders involved in the research, development, and marketing of prosthetic limb medical devices used by veteran amputees. A specific goal is to engage veteran amputees who use prosthetic limb medical devices and hear their views on these devices so that these perspectives may be considered in the total product life cycle of prosthetic limb devices.
- Date, Time and Location
- Federal Register Notice
- Registration
- Contact Us
Date, Time and Location
This meeting will be held October 31, 2016, beginning at 9:00 a.m. – 4:00 p.m. at the following location:
FDA White Oak Campus
10903 New Hampshire Avenue
Bldg. 31, Room 1503 (the Great Room)
Silver Spring, MD, 20993
- FDA Campus Information
The meeting will be webcast. Registration is not required to view the webcast, and the webcast link will be available on this web page after October 21, 2016.
Federal Register Notice
The Federal Register notice announcing this public meeting and containing other information is available here:
Registration to Attend the Workshop
If you wish to attend this Workshop, you must register by 4:00 p.m. on October 24, 2016.
There is no fee to register for the Workshop and registration will be on a first-come, first-served basis. Early registration is recommended because seating is limited.
If you wish to make an oral presentation during any of the open comment sessions at the meeting you must indicate this at the time of registration. FDA requests that presentations focus on the areas defined in the Federal Register Notice. You should also identify which discussion topic you wish to address in your presentation. In order to keep each open session focused on the discussion topic at hand, each oral presentation should address only one discussion topic. FDA will do its best to accommodate requests to speak.
Contact Us
If you require special accommodations due to a disability, or need additional information regarding registration, please contact Susan Monahan, Office of Communication and Education Programs, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Avenue, Bldg. 32, Silver Spring, MD 20993, 301-796-5661, [email protected].
For questions regarding workshop content please contact:
Fabienne Santel, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Avenue, Bldg. 66, rm. 3502, Silver Spring, MD 20993, 301-796-9644, email: [email protected].