ATRISORB BIOABSORBABLE GUIDED TISSUE REGNERATION(GTR)

ATRISORB BIOABSORBABLE GUIDED TISSUE REGNERATION(GTR) is an FDA 510(k)-cleared medical device (K955838) 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 March 20, 1996. Regulation: 8.