Stryker Spine - FDA 510(k) Cleared Devices
Recent clearances: Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip, OZARK Cervical Plate System, Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip, Vitoss® BiModal Bioactive Bone Graft Substitute, Vitoss BBTrauma® Bioactive Bone Graft Substitute,Vitoss® BA2X Bioactive Bone Graft Substitute, Vitoss® Bioactive Bone Graft Substitute Pack,Vitoss® Bioactive Bone Graft Substitute, Vitoss® Foam Bone Graft Substitute, Vitoss® Bone Graft Substitute Filled Canister, Vitoss® Bone Graft Substitute, Vitoss® Bone Graft Substitute - Synthetic Cancellous Chips
74
Total
73
Cleared
0
Denied
FDA 510(k) Regulatory Record - Stryker Spine Neurology ✕
1 devices