Orthomet, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ORTHOMET HMC FEMORAL STEM COMPONENT, ORTHOMET TITANIUM HYBRID FEMORAL STEM, ORTHOMET ANATOMICALLY GUIDED CARPAL TUNNEL RELEASE SY
60
Total
41
Cleared
0
Denied
FDA 510(k) Regulatory Record - Orthomet, Inc. Ophthalmic ✕
1 devices