
Synthes (Usa)
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SYNTHES ANTERIOR TENSION BAND (ATB) SYSTEM is an FDA 510(k)-cleared medical device (K022791) manufactured by Synthes (Usa). This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 12, 2002. Regulation: 8.