LEFORTE NEURO SYSTEM BONE PLATE

LEFORTE NEURO SYSTEM BONE PLATE is an FDA 510(k)-cleared medical device (K103778) manufactured by Jeil Medical Corporation. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 25, 2011. Regulation: 8.