Arco™-SA Lumbar Cage System

Arco™-SA Lumbar Cage System is an FDA 510(k)-cleared medical device (K173082) manufactured by Neurostructures, 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 March 28, 2018. Regulation: 8.