BIO-OSS, BIO-OSS BLOCKS AND BIO-OSS COLLAGEN— 510(k) K033815

Name: FDA 510(k) clearance K033815
Creator: U.S. Food and Drug Administration
Published: 2004-01-15

Substantially Equivalent

Geistlich-Pharma

FDA 510(k) clearance K033815 for BIO-OSS, BIO-OSS BLOCKS AND BIO-OSS COLLAGEN, Substantially Equivalent on 2004-01-15. Applicant: Geistlich-Pharma. Device class: 2.

Clearance details

Applicant: Geistlich-Pharma
Product code: Code NPM
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2003-12-09
Decision date: 2004-01-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, 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.