
Henke Sass Wolf of America, Inc.
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HENKE SASS WOLF OF AMERICA ARTHROSCOPE is an FDA 510(k)-cleared medical device (K080560) 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 March 17, 2008. Regulation: 8.