Medical Device Manufacturer · US , Clearwater , FL

Interbody Innovations, Llp - FDA 510(k) Cleared Devices

4 submissions · 1 cleared · Since 2005

Total

Cleared

Denied

Interbody Innovations, Llp has 1 FDA 510(k) cleared medical devices. Based in Clearwater, US.

Historical record: 1 cleared submissions from 2005 to 2008. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Interbody Innovations, Llp

4 devices

1-4 of 4