Globus Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ACTIFY™ Total Knee System, ACTIFY™ 3D Total Knee System (ACTIFY MC Tibial Insert), SCRIPT™ Rods, CREO™ Stabilization System, REVERE® Stabilization System, REVERE® 4.5 Stabilization System, NuVasive Reline™ System, SCRIPT™ Implant System
173
Total
170
Cleared
0
Denied
FDA 510(k) Regulatory Record - Globus Medical, Inc. General & Plastic Surgery ✕
2 devices