Asnis® III Cannulated Screw System and Asnis® PRO Cannulated Screw System

Asnis® III Cannulated Screw System and Asnis® PRO Cannulated Screw System is an FDA 510(k)-cleared medical device (K213199) manufactured by Stryker GmbH. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 10, 2022. Regulation: 8.