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FDA 510(k) Application Details - K203701
Device Classification Name
Implant, Endosseous, Root-Form
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510(K) Number
K203701
Device Name
Implant, Endosseous, Root-Form
Applicant
Ivory Super Holdco Inc. / Zest Anchors LLC
2875 Loker Avenue East
Carlsbad, CA 92010 US
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Contact
Marysa Loustalot
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Regulation Number
872.3640
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Classification Product Code
DZE
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More FDA Info for this Product Code
Date Received
12/18/2020
Decision Date
04/15/2021
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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