ALLOTROPAT/HEYLTEX CORP. BONE GRAFTING DENSE HYDRO— 510(k) K850012

Name: FDA 510(k) clearance K850012
Creator: U.S. Food and Drug Administration
Published: 1985-04-22

Substantially Equivalent

Heyltex Corp.

FDA 510(k) clearance K850012 for ALLOTROPAT/HEYLTEX CORP. BONE GRAFTING DENSE HYDRO, Substantially Equivalent on 1985-04-22. Applicant: Heyltex Corp.. Device class: 2.

Clearance details

Applicant: Heyltex Corp.
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 1985-01-02
Decision date: 1985-04-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

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