APF POROUS COATED LINE EXTENSION

APF POROUS COATED LINE EXTENSION is an FDA 510(k)-cleared medical device (K984154) manufactured by Biomet, 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 10, 1999. Regulation: 8.