Intermedics Orthopedics - FDA 510(k) Cleared Devices
Recent clearances: NATURAL-HIP SYSTEM POROUS STEM WITH HA/CSTI, NATURAL-KNEE II REVISION FEMORAL SPACER LUGS, NATURAL-HIP SYSTEM COCR REVISION STEM
108
Total
82
Cleared
0
Denied
FDA 510(k) Regulatory Record - Intermedics Orthopedics General & Plastic Surgery ✕
3 devices