NEXUS ACETABULAR CUP

NEXUS ACETABULAR CUP is an FDA 510(k)-cleared medical device (K905408) manufactured by Dow Corning Wright. 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 28, 1991. Regulation: 8.