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Reimbursement / Regulatory

Baxter Gains FDA Clearance for Bone Graft Substitute -

 

Baxter International was granted FDA 510(k) clearance to market Actifuse Flow bone graft substitute, offered in a prepackaged delivery syringe for precise placement into small bony voids or gaps.U.S. launch is expected by 4Q18. (Baxter International, 9/7/18).