Mini Cannulated Headed and Headless Screw Set

Mini Cannulated Headed and Headless Screw Set is an FDA 510(k)-cleared medical device (K183104) 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 June 9, 2019. Regulation: 8.