K232170
- 510(k) number
- K232170
- Device name
- Ti Link Abutment
- Applicant
- Izenimplant Co., Ltd. KR
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2024-01-12
- Date received
- 2023-07-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K232170.pdf
Official FDA record: K232170
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.