DT MedTech Announces Revision Procedures with H2 Ankle

DT MedTech announced successful ankle revision procedures with the Hintermann Series H2™ Tibial Assembly component and PE inlay.

U.S. and ex-U.S. sales and distribution will commence at the end of 1Q18 through HealthLink Europe.

The H2 device received FDA 510(k) clearance in 4Q17, and initial total ankle procedures occurred earlier this...

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Julie Vetalice is ORTHOWORLD's Editorial Assistant. She has covered the orthopedic industry for over 20 years, having joined the company in 1999.

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