Modulift Vertebral Body Replacement (VBR) System

Modulift Vertebral Body Replacement (VBR) System is an FDA 510(k)-cleared medical device (K172032) manufactured by Aesculap Implants Systems, 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 November 19, 2017. Regulation: 8.