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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 K801524
Device Name ZEST PLANT
Applicant
Zest Anchors, Inc.
4221 Richmond Rd., NW
Walker,  MI  49534
Correspondent
Zest Anchors, Inc.
4221 Richmond Rd., NW
Walker,  MI  49534
Regulation Number872.3640
Classification Product Code
DZE  
Date Received07/01/1980
Decision Date 07/21/1980
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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