
Zimmer Spine, Inc.
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TRINICA ANTERIOR LUMBAR PLATE SYSTEM is an FDA 510(k)-cleared medical device (K061353) manufactured by Zimmer Spine, 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 29, 2006. Regulation: 8.