K251497
- 510(k) number
- K251497
- Device name
- Elos Accurate Hybrid Base
- Applicant
- Elos Medtech Pinol A/S DK
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2025-10-16
- Date received
- 2025-05-15
- 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: K251497.pdf
Official FDA record: K251497
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.