CREED™ Cannulated Screws

CREED™ Cannulated Screws is an FDA 510(k)-cleared medical device (K223847) manufactured by Glw, Inc.. 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 24, 2023. Regulation: 8.