Centric Medical Gains FDA Clearance for Cannulated Screw in Foot/Ankle

Centric Medical received expanded FDA 510(k) clearance to market its Cannulated Screw Internal Fixation System in foot/ankle reconstruction.

New options for the line, which received its first 510(k) clearance in 2015, include indications specifically for the forefoot in 2.0, 2.5 and 3.0mm diameters with headed and headless designs. The initial...

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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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