Class Class II
VEA Align; spineEOS (K251747)
Description
VEA Align; spineEOS by Eos Imaging, an FDA 510(k) cleared radiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK251747
Clearance Date2025-08-15
Clearance TypeTraditional
Product CodeQIH
Regulation Number892.2050
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K251747
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. VEA Align; spineEOS (K251747) cites 3 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K240582 | VEA Align; spineEOS | Eos Imaging | 2024 |
| K202394 | EOSedge | Eos Imaging | 2020 |
| K152788 | EOS System | Eos Imaging | 2015 |
Trace the full predicate network for K251747
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.