Lumbar Interbody Fusion System (OLLIF)

Lumbar Interbody Fusion System (OLLIF) is an FDA 510(k)-cleared medical device (K173947) manufactured by Advanced Research Medical, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 24, 2018. Regulation: 8.