CITRESPLINE and CITRELOCK ACL Implants

CITRESPLINE and CITRELOCK ACL Implants is an FDA 510(k)-cleared medical device (K210239) manufactured by Acuitive Technologies, 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 February 23, 2021. Regulation: 8.