DIVERGENCE-L Anterior/Oblique Lumbar Fusion System

DIVERGENCE-L Anterior/Oblique Lumbar Fusion System is an FDA 510(k)-cleared medical device (K150135) manufactured by Medtronic Sofamor Danek USA, 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 10, 2015. Regulation: 8.