Medical Device Manufacturer · US , Washington , DC

Spineworks, LLC - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2005

Total

Cleared

Denied

Spineworks, LLC has 4 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 4 cleared submissions from 2005 to 2014. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Spineworks, LLC

4 devices

1-4 of 4