ACROMED ILIAC SCREW

ACROMED ILIAC SCREW is an FDA 510(k)-cleared medical device (K884161) manufactured by Buckman Co., 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 May 2, 1989. Regulation: 8.