VLIFT-s Vertebral Body Replacement System

VLIFT-s Vertebral Body Replacement System is an FDA 510(k)-cleared medical device (K183071) manufactured by Stryker Spine. 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 9, 2019. Regulation: 8.