The Food and Drug Administration (FDA) announced the following “CDRH Veteran Amputee Device Workshop.” The purpose of this workshop was to engage all stakeholders involved in the research, development, and marketing of prosthetic limb medical devices used by veteran amputees. A specific goal was 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
- Webcast
- Agenda
- Registration
- Contact Us
FDA Campus Information
Federal Register Notice
The Federal Register notice announcing this public meeting and containing other information is available here:
Part 2
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].