Enovis’ reverse glenoid system earns FDA clearance

Enovis earned FDA 510(k) clearance for its AltiVate reverse glenoid system, the devicemaker said July 12.

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The clearance expands the company’s glenoid implant offering of the AltiVate reverse shoulder system to include modular, augmented baseplates, according to a news release.

Mark Frankle, MD, performed the first case with the new system at Tampa (Fla.) General Hospital on July 8.

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