VARILIFT-L INTERBODY FUSION DEVICE

VARILIFT-L INTERBODY FUSION DEVICE is an FDA 510(k)-cleared medical device (K131296) 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 September 2, 2013. Regulation: 8.