PERIOGLAS- BIOGLASS BONE GRAFT PARTICULATE— 510(k) K992416

Name: FDA 510(k) clearance K992416
Creator: U.S. Food and Drug Administration
Published: 1999-10-15

Substantially Equivalent

Usbiomaterials Corp.

FDA 510(k) clearance K992416 for PERIOGLAS- BIOGLASS BONE GRAFT PARTICULATE, Substantially Equivalent on 1999-10-15. 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: 1999-07-20
Decision date: 1999-10-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Alachua, FL, US

Download summary PDF View on FDA.gov ↗

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