
Regeneration Technologies, Inc.
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STERLING CANCELLOUS CHIPS; STERLING CANCELLOUS CUBES is an FDA 510(k)-cleared medical device (K051615) manufactured by Regeneration Technologies, 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 14, 2005. Regulation: 8.