Wright Brings New Biologic To U.S. Ortho Space With Augment Approval

The Augment biologic-based device was approved for use in ankle and hindfoot fusions after overcoming multiple regulatory challenges.

Wright Medical Group NV overcame vendor quality challenges to gain FDA approval for its biologic-based Augment bone graft for aiding ankle/hindfoot fusion surgeries, opening up a $300 million U.S. market opportunity. The firm announced the approval Sept. 1. It's the first indication for a product platform that Wright hopes to extend to soft-tissue markets with even bigger potential.

The Augment platform combines tricalcium phosphate granules and recombinant human platelet-derived growth factor (rhPDGF) to stimulate healing following fusion

More from Archive

More from Medtech Insight