Medical Device Manufacturer · US , Jacksonville , FL

Biomet Micofixation - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2021

Total

Cleared

Denied

Biomet Micofixation has 3 FDA 510(k) cleared medical devices. Based in Jacksonville, US.

Last cleared in 2022. Active since 2021. Primary specialty: Orthopedic.

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

FDA 510(k) cleared devices by Biomet Micofixation

3 devices

1-3 of 3