REDAPT Sleeved Monolithic Revision Stems

REDAPT Sleeved Monolithic Revision Stems is an FDA 510(k)-cleared medical device (K162303) manufactured by Smith & Nephew, 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 April 30, 2017. Regulation: 8.