OsteoCentric Bone Plate and Screw System

OsteoCentric Bone Plate and Screw System is an FDA 510(k)-cleared medical device (K190430) manufactured by Osteocentric Trauma. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 21, 2019. Regulation: 8.