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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 K110640
Device Name ATLANTIS ABUTMENT FOR CAMLOG IMPLANT, DUPLICATE ABUTMENT, LATER ABUTMENT
Applicant
ASTRA TECH, INC.
8944 TAMAROA TERR.
SKOKIE,  IL  60076
Applicant Contact BETSY A BROWN
Correspondent
ASTRA TECH, INC.
8944 TAMAROA TERR.
SKOKIE,  IL  60076
Correspondent Contact BETSY A BROWN
Regulation Number872.3630
Classification Product Code
NHA  
Date Received03/04/2011
Decision Date 06/10/2011
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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