Medical Device Manufacturer · US , Westlake , OH

Spinal Edge, LLC - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2006

Total

Cleared

Denied

Spinal Edge, LLC has 3 FDA 510(k) cleared medical devices. Based in Westlake, US.

Historical record: 3 cleared submissions from 2006 to 2010. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Spinal Edge, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Spinal Edge, LLC

3 devices

1-3 of 3