
Coalign Innovations, Inc.
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ACCULIF TL AND PL CAGE is an FDA 510(k)-cleared medical device (K123752) manufactured by Coalign Innovations, 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 January 13, 2013. Regulation: 8.