Virtual Public Workshop – Orthopedic Device Postmarket Review The U.S. Food and Drug Administration (FDA) is announcing a virtual public workshop titled Orthopedic Device Postmarket Review. The purpose of this virtual workshop is to share information on medical device postmarket activities for orthopedic devices. All stakeholders, including members of the orthopedic community, device manufacturers, regulatory affairs professionals, clinicians, patients, and the general public, are welcome to attend. - Virtual Workshop Date: June 10, 2021 from 8:30 a.m. to 4:00 p.m. ET
- Location: The meeting will be held by webcast only.
- Registration Deadline: June 8, 2021 by 4:00 p.m. ET
Important Deadlines - May 14, 2021: Request special accommodations for the virtual workshop.
- June 8, 2021: Register to attend the virtual workshop.
- July 12, 2021: Submit written comments to the docket (FDA-2021-N-0414).
Questions? If you have questions about this virtual public workshop, contact Sahlee Sabala at OHT6-Feedback@fda.hhs.gov. |
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