K240603
- 510(k) number
- K240603
- Device name
- Ti-Base & Master Fix
- Applicant
- Arum Dentistry Co., Ltd. KR
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2024-06-05
- Date received
- 2024-03-04
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K240603.pdf
Official FDA record: K240603
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.