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Medical Devices / Submissions and Approvals

FDA Clears Centric Medical Cannulated Screw System

Jan. 25, 2018

The FDA gave 510(k) clearance to Life Spine’s Centric Medical division for its Cannulated Screw Internal Fixation System.

The multi-component, titanium alloy fixation system is intended for use in foot and ankle reconstruction procedures.

It provides a variety of diameters and lengths with head and headless designs.

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