![]() Demineralized bone matrices (DBM) regulated as medical devices by the FDA (e.g.Synthetic bone graft extenders (e.g., Attrax Scaffold (NuVasive), Formagraft (NuVasive), Mastergraft (Medtronic), Vitoss (Stryker), Actifuse (Baxter), nanOss (RTI Surgical), Fibergraft (Prosidyan/Depuy Synthes), ChronOs (Depuy Synthes)).Bone morphogenetic protein (BMP) (e.g., Infuse (Medtronic)).Use of any bone graft that is not cleared by the applicable regulatory body for use within interbody implants. Understands the conditions of enrollment, is willing to follow medical advice including postoperative activity restrictions per the surgeon's standard of care, and is willing to sign an informed consent form to participate in the study.Able to undergo surgery based on physical exam, medical history, and surgeon judgment. ![]()
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