Pro-Link® & Pro-Link® Ti Barbs Cervical Spacer System

Pro-Link® & Pro-Link® Ti Barbs Cervical Spacer System is an FDA 510(k)-cleared medical device (K231704) manufactured by Life Spine, 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 October 18, 2023. Regulation: 8.