FORTOSS VITAL BONE GRAFT SUBSTITUTE— 510(k) K050170

Name: FDA 510(k) clearance K050170
Creator: U.S. Food and Drug Administration
Published: 2005-08-26

Substantially Equivalent

Biocomposites, Ltd.

FDA 510(k) clearance K050170 for FORTOSS VITAL BONE GRAFT SUBSTITUTE, Substantially Equivalent on 2005-08-26. Applicant: Biocomposites, Ltd.. Device class: 2.

Clearance details

Applicant: Biocomposites, Ltd.
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2005-01-26
Decision date: 2005-08-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Keele, GB

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.