ACUFEX MENISCAL RASPS

ACUFEX MENISCAL RASPS is an FDA 510(k)-cleared medical device (K932460) manufactured by Acufex Microsurgical, 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 March 21, 1994. Regulation: 8.