Spinal Kinetics / Orthofix / Seaspine - FDA 510(k) Cleared Devices
Recent clearances: M6-C™ Single Use, Disposable Instrumentation
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Spinal Kinetics / Orthofix / Seaspine Orthopedic ✕
1 devices