
Spine View, Inc.
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SPINEVU ENDOSCOPIC SPINE SYSTEM (SESS), SPINEVU MINISCOPE is an FDA 510(k)-cleared medical device (K081051) 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 6, 2008. Regulation: 8.