VEA Align; spineEOS— 510(k) K251747
Substantially EquivalentEos Imaging
FDA 510(k) clearance K251747 for VEA Align; spineEOS, Substantially Equivalent on 2025-08-15. Applicant: Eos Imaging.
Clearance details
- Applicant
- Eos Imaging
- Product code
- Code QIH
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Paris, FR
Data sourced from openFDA. This site is unofficial and independent of the FDA.