Zimmer Cas - FDA 510(k) Cleared Devices
Recent clearances: IASSIST KNEE SYSTEM, CAS PSI SHOULDER, NAVITRACK SYSTEM - OS KNEE UNIVERSAL, CAS SAME INCISION TIBIA REFERENCE
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Zimmer Cas Orthopedic ✕
3 devices