PROFORM POROUS ACETABULAR ASSEMBLY

PROFORM POROUS ACETABULAR ASSEMBLY is an FDA 510(k)-cleared medical device (K950827) manufactured by Stelkast Company. 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 17, 1995. Regulation: 8.