FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

Paltop Conical Implant System

K Number: K220200 · Decision May 25, 2022
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
7
Review Days
121

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Basic Information

Device Name
Paltop Conical Implant System
K Number
K220200
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Paltop Advanced Dental Solutions, Ltd.
Date Received
January 24, 2022
Decision Date
May 25, 2022
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DZE), ordered by most recent decision date.

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Other Clearances by Paltop Advanced Dental Solutions, Ltd.

K Number Device Name
K243983 Paltop Dental Implant System
K232740 Paltop Short Implants
K210117 Paltop Narrow Implant
K130462 PALTOP NARROW IMPLANT, PALTOP SHORT IMPLANT
K131451 PALTOP DENTAL IMPLANT - STERILE ACCESSORIES
K112795 PALTOP DENTAL IMPLANT SYSTEM