Summit Spine Yellowstone Lumbar Interbody Fusion System

Summit Spine Yellowstone Lumbar Interbody Fusion System is an FDA 510(k)-cleared medical device (K170572) manufactured by Summit Spine. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 25, 2017. Regulation: 8.