JOHNSON & JOHNSON BIPOLAR ENDOPROTHESIS

JOHNSON & JOHNSON BIPOLAR ENDOPROTHESIS is an FDA 510(k)-cleared medical device (K873514) 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 23, 1987. Regulation: 8.