LACTOSORB MENISCAL SCREW

LACTOSORB MENISCAL SCREW is an FDA 510(k)-cleared medical device (K002020) manufactured by Biomet Manufacturing, Inc.. 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 24, 2000. Regulation: 8.