BONALIVE GRANULES AND BONALIVE PLATES— 510(k) K070055

Name: FDA 510(k) clearance K070055
Creator: U.S. Food and Drug Administration
Published: 2007-06-25

Substantially Equivalent

Vivoxid , Ltd.

FDA 510(k) clearance K070055 for BONALIVE GRANULES AND BONALIVE PLATES, Substantially Equivalent on 2007-06-25. Applicant: Vivoxid , Ltd.. Device class: 2.

Clearance details

Applicant: Vivoxid , Ltd.
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2007-01-04
Decision date: 2007-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Findley, MN, US

Download summary PDF View on FDA.gov ↗

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