NOVABONE-BIOGLASS BONE GRAFT PARTICULATE— 510(k) K000149

Name: FDA 510(k) clearance K000149
Creator: U.S. Food and Drug Administration
Published: 2000-02-07

Substantially Equivalent

Usbiomaterials Corp.

FDA 510(k) clearance K000149 for NOVABONE-BIOGLASS BONE GRAFT PARTICULATE, Substantially Equivalent on 2000-02-07. Applicant: Usbiomaterials Corp.. Device class: 2.

Clearance details

Applicant: Usbiomaterials Corp.
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2000-01-19
Decision date: 2000-02-07
Decision: Substantially Equivalent
Clearance type: Special
Location: Alachua, FL, US

Download summary PDF View on FDA.gov ↗

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