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

By Julie A. Vetalice

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 clearance addressed 0.5 to 7.5mm diameters indicated for midfoot and hindfoot, headed and headless.

Source: Centric Medical


Product Labels: Trauma Ankle/Foot/Toe

Tags: 510(k) Clearance, Regulatory