K242025
- 510(k) number
- K242025
- Device name
- Elos Accurate® Hybrid Base
- Applicant
- Elos Medtech Pinol A/S DK
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2024-12-10
- Date received
- 2024-07-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K242025.pdf
Official FDA record: K242025
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.