MENISCAL SUTURE INSTRUMENTARIUM

MENISCAL SUTURE INSTRUMENTARIUM is an FDA 510(k)-cleared medical device (K940287) manufactured by Richard Wolf Medical Instruments Corp.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 21, 1994. Regulation: 8.