
Omni Surgical, LP Dba Spine360
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STINGRAY CERVICAL CAGE is an FDA 510(k)-cleared medical device (K122085) manufactured by Omni Surgical, LP Dba Spine360. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 16, 2012. Regulation: 8.