FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SATURNO(TM) OVERDENTURE IMPLANT SYSTEM

K Number: K133327 · Decision Jun 25, 2014
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
12
Review Days
239

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Basic Information

Device Name
SATURNO(TM) OVERDENTURE IMPLANT SYSTEM
K Number
K133327
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zest Anchors, LLC
Date Received
October 29, 2013
Decision Date
June 25, 2014
Product Code
DZE
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DZE Implant, Endosseous, Root-Form

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Other Clearances by Zest Anchors, LLC

K Number Device Name
K260555 LOCATOR® Angled Abutment
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K243272 LOCATOR Angled Abutment
K233587 LOCATOR Angled Abutment (Various)
K220252 High Retention Attachment System
K213391 High Retention Attachment System
K191619 TurboTemp EZ
K151789 LOCATOR F-Tx Attachment System
K140570 CHAIRSIDE ATTACHMENT PROCESSING MATERIAL
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