
Collagen Matrix, Inc.
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Porcine Anorganic Bone Mineral in Delivery Applicator is an FDA 510(k)-cleared medical device (K162158) manufactured by Collagen Matrix, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 8, 2017. Regulation: 8.