K240582
- 510(k) number
- K240582
- Device name
- VEA Align; spineEOS
- Applicant
- Eos Imaging FR
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2024-06-25
- Date received
- 2024-03-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K240582.pdf
Official FDA record: K240582
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.