VARIAX 2 ONE THIRD TUBULAR PLATING SYSTEM

VARIAX 2 ONE THIRD TUBULAR PLATING SYSTEM is an FDA 510(k)-cleared medical device (K141204) 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 June 19, 2014. Regulation: 8.