
Ultrazonix Dnt AB
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ULTRAZONIX SPINE MINIMAL-INVASIVE DISC SYSTEM is an FDA 510(k)-cleared medical device (K060346) manufactured by Ultrazonix Dnt AB. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 21, 2006. Regulation: 8.