Medical Device Manufacturer · US , San Diego , CA

Seaspine - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2003

Total

Cleared

Denied

Seaspine has 5 FDA 510(k) cleared medical devices. Based in San Diego, US.

Historical record: 5 cleared submissions from 2003 to 2004. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Seaspine

5 devices

1-5 of 5