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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Alloy, Metal, Base
510(k) Number K900117
Device Name STELLITE COBALT/CHROMIUM BASE METAL ALLOY
Applicant
D.C. Dental Specialties
2007 Wilshire Blvd.
Suite 813-815
Los Angeles,  CA  90057
Applicant Contact DENZIL W CHESNEY
Correspondent
D.C. Dental Specialties
2007 Wilshire Blvd.
Suite 813-815
Los Angeles,  CA  90057
Correspondent Contact DENZIL W CHESNEY
Regulation Number872.3710
Classification Product Code
EJH  
Date Received01/09/1990
Decision Date 04/02/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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