CoreLink® M3™ Stand-Alone Anterior Lumbar System

CoreLink® M3™ Stand-Alone Anterior Lumbar System is an FDA 510(k)-cleared medical device (K180814) manufactured by Corelink, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 9, 2018. Regulation: 8.