FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

KATANA Zirconia ONE For IMPLANT

K Number: K233285 · Decision May 24, 2024
Classifications
1
FEI Numbers
390
Registration Numbers
390
Same Product Code
672
Applicant Total
14
Review Days
238

Basic Information

Device Name
KATANA Zirconia ONE For IMPLANT
K Number
K233285
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kuraray Noritake Dental Inc.
Date Received
September 29, 2023
Decision Date
May 24, 2024
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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