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

Telio CAD Abutment Solutions

K Number: K151564 · Decision Sep 21, 2015
Classifications
1
FEI Numbers
390
Registration Numbers
390
Same Product Code
672
Applicant Total
19
Review Days
103

Basic Information

Device Name
Telio CAD Abutment Solutions
K Number
K151564
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
IVOCLAR VIVADENT AG
Date Received
June 10, 2015
Decision Date
September 21, 2015
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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