
Arthro-Dif
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ACROSSPINE PEDICLE SCREW SYSTEM is an FDA 510(k)-cleared medical device (K141695) manufactured by Arthro-Dif. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 29, 2014. Regulation: 8.

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