
Arthrex, Inc.
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Arthrex Synergy UHD4 System is an FDA 510(k)-cleared medical device (K153218) manufactured by Arthrex, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 11, 2016. Regulation: 8.