HYDROCISION ARTHROJET SYSTEM

HYDROCISION ARTHROJET SYSTEM is an FDA 510(k)-cleared medical device (K982266) manufactured by Hydrocision, 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 24, 1998. Regulation: 8.