LEUCADIA AUTOLOK™ Pedicle Screw System

LEUCADIA AUTOLOK™ Pedicle Screw System is an FDA 510(k)-cleared medical device (K182339) manufactured by Clearview Orthopedic Development, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 11, 2018. Regulation: 8.