Life Spine Lumbar Fixation System (SENTRY)

Life Spine Lumbar Fixation System (SENTRY) is an FDA 510(k)-cleared medical device (K180166) 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 June 21, 2018. Regulation: 8.