ATRISORB-D FREEFLOW BIOABSORBABLE GUIDED TISSUE REGENERATION (GTR) BARRIER WITH 4% DOXYCYCLINE— 510(k) K994137

Name: FDA 510(k) clearance K994137
Creator: U.S. Food and Drug Administration
Published: 2000-09-13

Substantially Equivalent

Atrix Laboratories, Inc.

FDA 510(k) clearance K994137 for ATRISORB-D FREEFLOW BIOABSORBABLE GUIDED TISSUE REGENERATION (GTR) BARRIER WITH 4% DOXYCYCLINE, Substantially Equivalent on 2000-09-13. Applicant: Atrix Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Atrix Laboratories, Inc.
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 1999-12-07
Decision date: 2000-09-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Collins, CO, US

Download summary PDF View on FDA.gov ↗

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