Medical Device Manufacturer · US , Cincinnati , OH

Vertebration,Inc - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2007

Total

Cleared

Denied

Vertebration,Inc has 2 FDA 510(k) cleared medical devices. Based in Cincinnati, US.

Historical record: 2 cleared submissions from 2007 to 2009. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Vertebration,Inc

2 devices

1-2 of 2