
Difusion Technologies
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DIFUSION TECHNOLOGIES XIPHOS INTERBODY FUSION SYSTEM is an FDA 510(k)-cleared medical device (K100042) manufactured by Difusion Technologies. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 30, 2010. Regulation: 8.