MAXFIRE MARXMEN MENISCAL REPAIR DEVICE

MAXFIRE MARXMEN MENISCAL REPAIR DEVICE is an FDA 510(k)-cleared medical device (K111564) manufactured by Biomet Sports Medicine. 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 15, 2011. Regulation: 8.