ATRISORB BIOABSORBABLE GUIDED TISSUE REGNERATION(GTR)— 510(k) K955838

Name: FDA 510(k) clearance K955838
Creator: U.S. Food and Drug Administration
Published: 1996-03-21

Substantially Equivalent

Atrix Laboratories, Inc.

FDA 510(k) clearance K955838 for ATRISORB BIOABSORBABLE GUIDED TISSUE REGNERATION(GTR), Substantially Equivalent on 1996-03-21. Applicant: Atrix Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Atrix Laboratories, Inc.
Product code: Code NPK
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 1995-12-22
Decision date: 1996-03-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Collins, CO, US

Download summary PDF View on FDA.gov ↗

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