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Vascular Technology Incorporated
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VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000; VTI SKULL SCREW, MODEL 22001 is an FDA 510(k)-cleared medical device (K002990) manufactured by Vascular Technology Incorporated. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 5, 2000. Regulation: 8.