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

Duranext Abutments

K Number: K200355 · Decision Jul 22, 2020
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
1
Review Days
160

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Basic Information

Device Name
Duranext Abutments
K Number
K200355
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Elegant Dental Corp.
Date Received
February 13, 2020
Decision Date
July 22, 2020
Product Code
NHA
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
NHA Abutment, Implant, Dental, Endosseous

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