Stryker Spine is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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
Stryker Spine has 73 FDA 510(k) cleared orthopedic devices. Based in Allendale, US.
Latest FDA clearance: Apr 2026. Active since 2004.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Stryker as regulatory consultant.
FDA 510(k) Regulatory Record - Stryker Spine
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