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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 K024214
Device Name KAVO EVEREST TITANBLANK
Applicant
Kavo America
340 E. Main St.
Lake Zurich,  IL  60047
Applicant Contact JOHN R FRANZ
Correspondent
Kavo America
340 E. Main St.
Lake Zurich,  IL  60047
Correspondent Contact JOHN R FRANZ
Regulation Number872.3710
Classification Product Code
EJH  
Date Received12/20/2002
Decision Date 03/12/2003
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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