K233285
- 510(k) number
- K233285
- Device name
- KATANA Zirconia ONE For IMPLANT
- Applicant
- Kuraray Noritake Dental, Inc. JP
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2024-05-24
- Date received
- 2023-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K233285.pdf
Official FDA record: K233285
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.