HSW GMBH ARTHROSCOPE

HSW GMBH ARTHROSCOPE is an FDA 510(k)-cleared medical device (K962075) manufactured by Henke Sass Wolf of America, 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 January 16, 1997. Regulation: 8.