
X-Spine Systems, Inc.
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SILEX SACROILIAC JOINT FUSION SYSTEM is an FDA 510(k)-cleared medical device (K123702) manufactured by X-Spine Systems, 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 March 10, 2013. Regulation: 8.