Glw, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CREED™ Cannulated Screws, Artemis Proximal Femoral Nail System, Artemis Proximal Femoral Nail System
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Glw, Inc. Orthopedic ✕
3 devices