Lumbar Interbody Fusion System (ALIF, PLIF, LLIF, TPLIF)

Lumbar Interbody Fusion System (ALIF, PLIF, LLIF, TPLIF) is an FDA 510(k)-cleared medical device (K160663) manufactured by Evolution Spine, 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 November 15, 2016. Regulation: 8.