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Medical Devices / Submissions and Approvals

FDA Clears Centric Medical Cannulated Screw System

Jan. 25, 2018
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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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