
Atrix Laboratories, Inc.
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ATRISORB-D FREEFLOW BIOABSORBABLE GUIDED TISSUE REGENERATION (GTR) BARRIER WITH 4% DOXYCYCLINE is an FDA 510(k)-cleared medical device (K994137) manufactured by Atrix Laboratories, 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 September 12, 2000. Regulation: 8.