FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇰 Denmark

Abutment Design

K Number: K200100 · Decision Oct 7, 2020
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
7
Applicant Total
8
Review Days
265

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Basic Information

Device Name
Abutment Design
K Number
K200100
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
3Shape A/S
Date Received
January 16, 2020
Decision Date
October 7, 2020
Product Code
PNP
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
PNP Dental Abutment Design Software For Dental Laboratory

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K Number Device Name
K191911 3Shape Splint Design
K180941 Ortho System
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K151455 3Shape Abutment Designer Software
K152086 3Shape Ortho System