MODIFICATION TO: OSTEOGRAF/N-700— 510(k) K072058

Name: FDA 510(k) clearance K072058
Creator: U.S. Food and Drug Administration
Published: 2007-08-03

Substantially Equivalent

Dentsply Interntional

FDA 510(k) clearance K072058 for MODIFICATION TO: OSTEOGRAF/N-700, Substantially Equivalent on 2007-08-03. Applicant: Dentsply Interntional. Device class: 2.

Clearance details

Applicant: Dentsply Interntional
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2007-07-26
Decision date: 2007-08-03
Decision: Substantially Equivalent
Clearance type: Special
Location: York, PA, 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.