FEMORAL CEMENT REMOVAL INSTRUMENTS
Feb 1987
16d
Kenneth J. Hoek, M.D., Inc. has 1 FDA 510(k) cleared medical devices. Based in Ukiah, US.
Historical record: 1 cleared submissions from 1987 to 1987. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Kenneth J. Hoek, M.D., Inc. Filter by specialty or product code using the sidebar.