K241722
- 510(k) number
- K241722
- Device name
- Elos Accurate® Hybrid Base; Elos Accurate® Customized Abutment
- Applicant
- Elos Medtech Pinol A/S DK
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2024-09-13
- Date received
- 2024-06-14
- 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: K241722.pdf
Official FDA record: K241722
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.