Class Class II
Aventus Thrombectomy System (K251189)
Description
Aventus Thrombectomy System by Inquis Medical, an FDA 510(k) cleared cardiovascular device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK251189
Clearance Date2025-06-13
Clearance TypeTraditional
Product CodeQEW
Regulation Number870.5150
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K251189
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. Aventus Thrombectomy System (K251189) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K240117 | Aventus Thrombectomy System (IM-2001/IM-0002) | Inquis Medical | 2024 |
| K191710 | FlowTriever Retrieval/Aspiration System | Inari Medical | 2019 |
Trace the full predicate network for K251189
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.