Medical Device Manufacturer · US , Newtown Square , PA

Camber Spine - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2014

Total

Cleared

Denied

Camber Spine has 4 FDA 510(k) cleared medical devices. Based in Newtown Square, US.

Historical record: 4 cleared submissions from 2014 to 2015. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Camber Spine

4 devices

1-4 of 4