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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 K072878
Device Name MODIFICATION TO: LOCATOR IMPLANT ANCHOR
Applicant
Zest Anchors, Inc.
2061 Wineridge Pl
Escondido,  CA  92029
Applicant Contact RICHARD OVERTON
Correspondent
Zest Anchors, Inc.
2061 Wineridge Pl
Escondido,  CA  92029
Correspondent Contact RICHARD OVERTON
Regulation Number872.3630
Classification Product Code
NHA  
Date Received10/09/2007
Decision Date 12/03/2007
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
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