BATEMAN UPF-III BIPOLAR ENDOPROSTHESIS SYSTEM

BATEMAN UPF-III BIPOLAR ENDOPROSTHESIS SYSTEM is an FDA 510(k)-cleared medical device (K913632) manufactured by Kirschner Medical 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 November 12, 1991. Regulation: 8.