VariLift-L Interbody Fusion Device

VariLift-L Interbody Fusion Device is an FDA 510(k)-cleared medical device (K151900) manufactured by Wenzel Spine, 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 December 10, 2015. Regulation: 8.