CorticaLINK Spinal Fusion Platform

CorticaLINK Spinal Fusion Platform is an FDA 510(k)-cleared medical device (K173484) manufactured by Linkspine, 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 December 10, 2017. Regulation: 8.