THUNDERBOLT AND LANCER PEDICLE SCREW SYSTEMS

THUNDERBOLT AND LANCER PEDICLE SCREW SYSTEMS is an FDA 510(k)-cleared medical device (K132049) manufactured by Choicespine. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 14, 2014. Regulation: 8.