KLIMT™ Expandable Lumbar Interbody Fusion (LIF) Cage System

KLIMT™ Expandable Lumbar Interbody Fusion (LIF) Cage System is an FDA 510(k)-cleared medical device (K233947) manufactured by Ctl Medical Corporation. 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 9, 2024. Regulation: 8.