PERIOGLAS-BIOGLASS BONE GRAFT SUBSTITUTE— 510(k) K040278

Name: FDA 510(k) clearance K040278
Creator: U.S. Food and Drug Administration
Published: 2004-03-01

Substantially Equivalent

Novabone Products, LLC

FDA 510(k) clearance K040278 for PERIOGLAS-BIOGLASS BONE GRAFT SUBSTITUTE, Substantially Equivalent on 2004-03-01. Applicant: Novabone Products, LLC. Device class: 2.

Clearance details

Applicant: Novabone Products, LLC
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2004-02-05
Decision date: 2004-03-01
Decision: Substantially Equivalent
Clearance type: Special
Location: Alachua, FL, US

Download summary PDF View on FDA.gov ↗

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