Johnson & Johnson Orthopaedics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PFC MODULAR TOTAL KNEE SYSTEM, POROUS COATED SACRI, P.F.C. 2 TOTAL HIP SYSTEM POROUS COATED MODULAR FEMORAL COMPONENT, ULTIMA UNIPOLAR MODULAR HEAD
22
Total
19
Cleared
0
Denied
FDA 510(k) Regulatory Record - Johnson & Johnson Orthopaedics, Inc. General Hospital ✕
1 devices