ENZA-A Titanium ALIF

ENZA-A Titanium ALIF is an FDA 510(k)-cleared medical device (K173432) 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 April 17, 2018. Regulation: 8.