Integrity Spine Lumbar Interbody Fusion System

Integrity Spine Lumbar Interbody Fusion System is an FDA 510(k)-cleared medical device (K151819) manufactured by Integrity Spine Lumbar Interbody Fusion System. 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 9, 2015. Regulation: 8.