DT MedTech gets FDA premarket approval for ankle replacement system

The U.S. Food and Drug Administration Wednesday granted premarket approval to Baltimore-based DT MedTech LLC for its Hintermann Series H3 Total Ankle Replacement System. The H3 is a three-piece, mobile-bearing implant for use as a non-cemented implant to replace a painful arthritic ankle joint because of primary osteoarthritis, post-traumatic osteoarthritis or arthritis secondary to inflammatory disease. The ...

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