POWERCUT SURGICAL SYSTEM, BLADES, AND ACCESSORIES

POWERCUT SURGICAL SYSTEM, BLADES, AND ACCESSORIES is an FDA 510(k)-cleared medical device (K904720) manufactured by Baxter Healthcare 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 October 25, 1990. Regulation: 8.