OSTEOGRAF/AR AND OSTEOGRAF/AR+— 510(k) K862324

Substantially Equivalent

Coors Biomedical Co.

FDA 510(k) clearance K862324 for OSTEOGRAF/AR AND OSTEOGRAF/AR+, Substantially Equivalent on 1986-08-15. 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
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Lakewood, CO, US
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