WAGNER REVISION STEM (MODIFICATION)

WAGNER REVISION STEM (MODIFICATION) is an FDA 510(k)-cleared medical device (K953689) manufactured by Intermedics Orthopedics. 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 28, 1995. Regulation: 8.