K250081
- 510(k) number
- K250081
- Device name
- Atlantis® Abutments in Titanium
- Applicant
- Dentsply Sirona PA · US
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2025-04-11
- Date received
- 2025-01-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K250081.pdf
Official FDA record: K250081
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.