LEFORTE NEURO SYSTEM BONE PLATE AND SCREW

LEFORTE NEURO SYSTEM BONE PLATE AND SCREW is an FDA 510(k)-cleared medical device (K141452) manufactured by Jeil Medical Corporation. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 1, 2014. Regulation: 8.