ENZA-O Titanium Lateral Anterior Lumbar Interbody Fusion (ALIF)

ENZA-O Titanium Lateral Anterior Lumbar Interbody Fusion (ALIF) is an FDA 510(k)-cleared medical device (K221324) manufactured by Camber Spine Technologies. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 29, 2023. Regulation: 8.