HASTINGS BIPOLAR ENDOPROSTHESIS

HASTINGS BIPOLAR ENDOPROSTHESIS is an FDA 510(k)-cleared medical device (K842344) manufactured by Johnson & Johnson Professionals, 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 September 11, 1984. Regulation: 8.