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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 K203456
Device Name Straumann CARES M-Series CAD/CAM System
Applicant
Institut Straumann AG
Peter Merian-Weg 12
Basel,  CH CH-4002
Applicant Contact Gordon Dodds
Correspondent
Straumann USA, LLC
60 Minuteman Rd.
Andover,  ME  01810
Correspondent Contact Jennifer M Jackson
Regulation Number872.3630
Classification Product Code
NHA  
Subsequent Product Code
PNP  
Date Received11/23/2020
Decision Date 06/23/2021
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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