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# FDA Clears Centric Medical Foot Reconstruction Device
- URL: https://www.fdaweb.com/fda-clears-centric-medical-foot-reconstruction-device/
- Published: 2018-01-18T12:00:00.000Z
- Updated: 2026-09-14T23:14:55.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5140535

FDA has cleared a Centric Medical 510(k) for the Cannulated Screw Internal Fixation System for use in foot and ankle reconstruction procedures. The company says the streamlined multi-component system is made of titanium alloy and comes in a variety of diameters and lengths (2.0, 2.5, and 3.0 mm diameters with headed and headless designs). It complements the previously FDA-cleared range of 3.5-7.5mm diameters indicated for the midfoot and hindfoot.