CAPTIVATE® Compression Screws

CAPTIVATE® Compression Screws is an FDA 510(k)-cleared medical device (K222409) manufactured by Globus Medical, 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 September 7, 2022. Regulation: 8.