Stryker Spine - FDA 510(k) Cleared Devices
Recent clearances: Tritanium® C Anterior Cervical Cage, Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip, OZARK Cervical Plate System
75
Total
74
Cleared
0
Denied
FDA 510(k) Regulatory Record - Stryker Spine General & Plastic Surgery ✕
1 devices