AERIAL™ Interspinous Fixation

AERIAL™ Interspinous Fixation is an FDA 510(k)-cleared medical device (K180817) manufactured by Globus Medical, 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 May 20, 2018. Regulation: 8.