Medical Device Manufacturer · US , Parsippany , NJ

Biomet Trauma - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2007

Total

Cleared

Denied

Biomet Trauma has 7 FDA 510(k) cleared medical devices. Based in Parsippany, US.

Historical record: 7 cleared submissions from 2007 to 2009. Primary specialty: Orthopedic.

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

Biomet Trauma is one of 20712 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Biomet Trauma

7 devices

1-7 of 7