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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Abutment, Implant, Dental, Endosseous
510(k) Number K142167
Device Name MEDENTIKA ABUTMENT SYSTEM
Applicant
Medentika GmbH
12264 El Camino Real
Suite 400
San Diego,  CA  92130
Applicant Contact LINDA SCHULZ
Correspondent
Medentika GmbH
12264 El Camino Real
Suite 400
San Diego,  CA  92130
Correspondent Contact LINDA SCHULZ
Regulation Number872.3630
Classification Product Code
NHA  
Date Received08/06/2014
Decision Date 02/20/2015
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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