prodisc C SK, prodisc C Nova, and prodisc C Vivo Instruments

prodisc C SK, prodisc C Nova, and prodisc C Vivo Instruments is an FDA 510(k)-cleared medical device (K221848) manufactured by Centinel Spine, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 18, 2022. Regulation: 8.