Class Class II
Liberant Thrombectomy System (K250787)
Description
Liberant Thrombectomy System by Medtronic, Ireland, an FDA 510(k) cleared cardiovascular device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK250787
Clearance Date2025-06-11
Clearance TypeTraditional
Product CodeQEW
Regulation Number870.5150
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K250787
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. Liberant Thrombectomy System (K250787) cites 3 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K192981 | Indigo System Aspiration Catheter 12, Indigo Aspiration Sys... | Penumbra, Inc. | 2020 |
| K193244 | Indigo Aspiration System Lightning Aspiration Tubing | Penumbra, Inc. | 2020 |
| K142870 | Penumbra Embolectomy Aspiration System [INDIGO Aspiration S... | Penumbra, Inc. | 2015 |
Trace the full predicate network for K250787
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.