K241170
- 510(k) number
- K241170
- Device name
- Dynamic TiBase; TRI Screws
- Applicant
- Talladium España, SL ES
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2024-10-21
- Date received
- 2024-04-26
- 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: K241170.pdf
Official FDA record: K241170
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.