OSTEOGRAF/AR ALVEOLAR RID HYDROX, 18-40 MESH— 510(k) K861084

Name: FDA 510(k) clearance K861084
Creator: U.S. Food and Drug Administration
Published: 1986-04-30

Substantially Equivalent

Coors Biomedical Co.

FDA 510(k) clearance K861084 for OSTEOGRAF/AR ALVEOLAR RID HYDROX, 18-40 MESH, Substantially Equivalent on 1986-04-30. Applicant: Coors Biomedical Co.. Device class: 2.

Clearance details

Applicant: Coors Biomedical Co.
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 1986-03-21
Decision date: 1986-04-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lakewood, CO, US

Download summary PDF View on FDA.gov ↗

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