STELLITE COBALT/CHROMIUM BASE METAL ALLOY— 510(k) K900117

Name: FDA 510(k) clearance K900117
Creator: U.S. Food and Drug Administration
Published: 1990-04-02

Substantially Equivalent

D.C. Dental Specialties

FDA 510(k) clearance K900117 for STELLITE COBALT/CHROMIUM BASE METAL ALLOY, Substantially Equivalent on 1990-04-02. Applicant: D.C. Dental Specialties. Device class: 2.

Clearance details

Applicant: D.C. Dental Specialties
Product code: Code EJH
Device class: Class 2
Regulation: 21 CFR 872.3710
Advisory panel: Dental
Date received: 1990-01-09
Decision date: 1990-04-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, US

Download summary PDF View on FDA.gov ↗

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