K242607
- 510(k) number
- K242607
- Device name
- ScanDiags Ortho L-Spine MR-Q
- Applicant
- Scandiags AG CH
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2025-02-21
- Date received
- 2024-09-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K242607.pdf
Official FDA record: K242607
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.