Medical Device Manufacturer · US , St. Paul , MN

Synovis Surgical Innovations - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2003

Total

Cleared

Denied

Synovis Surgical Innovations has 8 FDA 510(k) cleared medical devices. Based in St. Paul, US.

Historical record: 8 cleared submissions from 2003 to 2013. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Synovis Surgical Innovations Filter by specialty or product code using the sidebar.

Synovis Surgical Innovations is one of 5263 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

Synovis Surgical Innovations — FDA 510(k) Products and Clearance History

8 devices

1-8 of 8