ADVANCED REVISION PRODUCT LINE EXTENSION

ADVANCED REVISION PRODUCT LINE EXTENSION is an FDA 510(k)-cleared medical device (K990030) manufactured by Wrightmedicaltechnologyinc. 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 2, 1999. Regulation: 8.