KeyLift™ Expandable Interlaminar Stabilization System

KeyLift™ Expandable Interlaminar Stabilization System is an FDA 510(k)-cleared medical device (K232484) manufactured by Flospine. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 18, 2023. Regulation: 8.