ACUFEX(R) ENDO-FEMORAL AIMER

ACUFEX(R) ENDO-FEMORAL AIMER is an FDA 510(k)-cleared medical device (K942846) 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 September 27, 1994. Regulation: 8.