K253315
- 510(k) number
- K253315
- Device name
- Straumann Variobase Abutments XC for Bridge/Bar
- Applicant
- Institut Straumann AG CH
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2026-01-22
- Date received
- 2025-09-30
- 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: K253315.pdf
Official FDA record: K253315
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.