AXSOS 3 TI LOCKING PLATE SYSTEM LINE EXTENSION

AXSOS 3 TI LOCKING PLATE SYSTEM LINE EXTENSION is an FDA 510(k)-cleared medical device (K133440) manufactured by Stryker Trauma AG. 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 17, 2013. Regulation: 8.