INSTRUMENT MAKAR PERFIX INTERFERENCE BONE SCREW

INSTRUMENT MAKAR PERFIX INTERFERENCE BONE SCREW is an FDA 510(k)-cleared medical device (K930980) manufactured by Instrument Makar, 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 February 9, 1994. Regulation: 8.