Birmingham Hip (BH) Dual Mobility Insert

Birmingham Hip (BH) Dual Mobility Insert is an FDA 510(k)-cleared medical device (K171934) 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 November 29, 2017. Regulation: 8.