Tenet Medical Engineering - FDA 510(k) Cleared Devices
Recent clearances: TENET MLTI-POSITIONING SURGICAL STIRRUP SYSTEM, TENET RADIOLUCENT HAND TABLE, TENET TIBIAL FRACTURE SUPPORT
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Tenet Medical Engineering General & Plastic Surgery ✕
2 devices