
Pisharodi Surgicals, Inc.
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UNIVERSAL MULTIAXIS (UNIMAX) PEDICLE SCREW SYSTEM is an FDA 510(k)-cleared medical device (K014302) manufactured by Pisharodi Surgicals, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 28, 2002. Regulation: 8.