Atrix Laboratories, Inc.

FDA Regulatory Profile

Atrix Laboratories, Inc. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 13, 2000.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K994137ATRISORB-D FREEFLOW BIOABSORBABLE GUIDED TISSUE REGENERATION (GTR) BARRIER WITH 4% DOXYCYCLINESeptember 13, 2000
K982865ATRISORB BIOABSORBABLE GUIDED TISSUE REGENERATION (GTR) BARRIER KITSeptember 8, 1998
K955838ATRISORB BIOABSORBABLE GUIDED TISSUE REGNERATION(GTR)March 21, 1996