
Spinefrontier, Inc.
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S-LIF INTERVERTEBRAL BODY FUSION DEVICE is an FDA 510(k)-cleared medical device (K092815) manufactured by Spinefrontier, 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 June 29, 2010. Regulation: 8.