VITALOCK SOLID BACKED ACETABULAR SHELL

VITALOCK SOLID BACKED ACETABULAR SHELL is an FDA 510(k)-cleared medical device (K952397) manufactured by Howmedica Corp.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 20, 1995. Regulation: 8.