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Stryker Spine · Class II · Cleared Aug 29, 2024

K-numberK242280
Device nameVitoss® 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
ApplicantStryker Spine
Product codeMQV
Device classClass II
Decision dateAug 29, 2024
DecisionSubstantially Equivalent
Regulation888.3045
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View the full FDA submission: accessdata.fda.gov

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