K231559
- 510(k) number
- K231559
- Device name
- Multi-Unit DAS System
- Applicant
- Talladium España, SL ES
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2023-11-17
- Date received
- 2023-05-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K231559.pdf
Official FDA record: K231559
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.