BIOGRAN BIOACTIVE GLASS SYNTHETIC BONE GRAFT MATERIAL— 510(k) K952922

Name: FDA 510(k) clearance K952922
Creator: U.S. Food and Drug Administration
Published: 1995-12-19

Substantially Equivalent

Orthovita Co.

FDA 510(k) clearance K952922 for BIOGRAN BIOACTIVE GLASS SYNTHETIC BONE GRAFT MATERIAL, Substantially Equivalent on 1995-12-19. Applicant: Orthovita Co.. Device class: 2.

Clearance details

Applicant: Orthovita Co.
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 1995-06-26
Decision date: 1995-12-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Princeton, NJ, US

Download summary PDF View on FDA.gov ↗

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