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
382
Registration Numbers
382
Same Product Code
708
Applicant Total
32
Review Days
238
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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 | Device Class | Medical Specialty |
|---|---|---|---|
| NHA | Abutment, Implant, Dental, Endosseous | FDA class 2 | Dental |
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