K251613
- 510(k) number
- K251613
- Device name
- SwissGraft X
- Applicant
- Geistlich Pharma AG CH
- Product code
- NPM — Bone Grafting Material, Animal Source
- Decision date
- 2025-06-26
- Date received
- 2025-05-27
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K251613.pdf
Official FDA record: K251613
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.