Biomet Micofixation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biomet Micofixation - FDA 510(k) Cleared Devices
Recent clearances: 2.1 x 255mm Drill, 22mm Stop, Pectus Blu Support Bar System, Biomet Microfixation RibFix Advantage System
3
Total
3
Cleared
0
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.
Regulatory submissions have been managed by MRC Global, LLC and MRC Global.
FDA 510(k) Regulatory Record - Biomet Micofixation
3 devices