
Jg Spine, LLC
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SUREFIX INTERSPINOUS FUSION SYSTEM is an FDA 510(k)-cleared medical device (K124014) manufactured by Jg Spine, 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 August 8, 2013. Regulation: 8.