
Renovis Surgical Technologies, LLC
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RENOVIS CANNULATED SCREW SYSTEM is an FDA 510(k)-cleared medical device (K113084) manufactured by Renovis Surgical Technologies, LLC. 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 8, 2011. Regulation: 8.