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Collegeville, Pa.-based Synergy Biomedical received FDA clearance for its BioSphere Putty for bone grafts.
Shelton, Conn.-based Spine Wave received FDA 510(k) clearance for its StaXx IB System, an intervertebral body fusion device.
In a recent retrospective study published in Spine, researchers analyzed the rate of infection seen in vertebral fusion patients that received irradiated cancellous allograft or iliac crest bone autograft.
Published in Spine
Leesburg, Va.-based K2M has launched a bone graft system, an expansion of its biologics offering.
Pioneer Surgical Technology announced its nanOss Bioactive bone graft has been successfully implanted into a human.
BioMimetic Therapeutics introduced the Augmatrix Biocomposite Bone Graft, a new bone graft substitute product line composed of carbonate-apatite and Type 1 collagen, according to a company news release.