
Kinetikos Medical, Inc.
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MODIFICATION TO UNIVERSAL TOTAL WRIST SYSTEM is an FDA 510(k)-cleared medical device (K020554) manufactured by Kinetikos Medical, 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 May 2, 2002. Regulation: 8.