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Spine View, Inc.
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SPINEVU ENDOSCOPIC SPINE SYSTEM (SESS) is an FDA 510(k)-cleared medical device (K121548) manufactured by Spine View, 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 August 15, 2012. Regulation: 8.