FDA Clears Osteoinductive Bone Graft Substitute From Wright Medical Group

The FDA has cleared Wright Medical Group’s Pro-Stim Injectable Osteoinductive Bone Graft Substitute, allowing a limited group of trial centers to validate pre-clinical findings in clinical use, according to a release from Wright Medical Group.

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The Pro-Stim graft provides surgeons with the osteoconductive base material derived from its Pro-Dense graft, which is a combination of calcium sulfate and calcium phosphate materials, but adds a high volume of osteoinductive demineralized bone matrix to the formulation.

A full roll-out in the United States and some international markets is planned for the second half of 2010.

Read Wright Medical Group’s release on the Pro-Stim bone graft substitute.

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