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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name implant, endosseous, root-form
510(k) Number K934668
Device Name ZEST IMPLANT ANCHOR ADVANCED GENERATION (DENTAL)
Applicant
ZEST ANCHORS, INC.
2061 WINERIDGE PL., SUITE 100
ESCONDIDO,  CA  92029
Applicant Contact PAUL ZUEST
Correspondent
ZEST ANCHORS, INC.
2061 WINERIDGE PL., SUITE 100
ESCONDIDO,  CA  92029
Correspondent Contact PAUL ZUEST
Regulation Number872.3640
Classification Product Code
DZE  
Date Received09/29/1993
Decision Date 06/22/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
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