BIOBAR, IMPLANTABLE BIODEGRADABLE COLLAGEN MEMBRANE FOR GUIDED BONE REGENERATION— 510(k) K001598

Name: FDA 510(k) clearance K001598
Creator: U.S. Food and Drug Administration
Published: 2000-08-22

Substantially Equivalent

Col-Bar , Ltd.

FDA 510(k) clearance K001598 for BIOBAR, IMPLANTABLE BIODEGRADABLE COLLAGEN MEMBRANE FOR GUIDED BONE REGENERATION, Substantially Equivalent on 2000-08-22. Applicant: Col-Bar , Ltd.. Device class: 2.

Clearance details

Applicant: Col-Bar , Ltd.
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2000-05-24
Decision date: 2000-08-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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