Vitality® Spinal Fixation System, Vitality®+ Power Instrument System

Vitality® Spinal Fixation System, Vitality®+ Power Instrument System is an FDA 510(k)-cleared medical device (K172275) manufactured by Zimmer Biomet Spine, 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 26, 2017. Regulation: 8.