Medical Device Manufacturer · US , Santa Barbara , CA

Ossacur AG - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2004

Total

Cleared

Denied

Ossacur AG has 4 FDA 510(k) cleared medical devices. Based in Santa Barbara, US.

Historical record: 4 cleared submissions from 2004 to 2006. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Ossacur AG Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ossacur AG

4 devices

1-4 of 4