STALIF TT INTERVERTEBRAL BODY FUSION SYSTEM

STALIF TT INTERVERTEBRAL BODY FUSION SYSTEM is an FDA 510(k)-cleared medical device (K073109) manufactured by Surgicraft , Ltd.. 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 3, 2008. Regulation: 8.