Class Class II
ClotTriever XL Catheter (41-102) (K242557)
Description
ClotTriever XL Catheter (41-102) by Inari Medical, Inc., an FDA 510(k) cleared cardiovascular device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK242557
Clearance Date2024-09-27
Clearance TypeSpecial
Product CodeQEW
Regulation Number870.5150
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242557
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. ClotTriever XL Catheter (41-102) (K242557) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K223210 | ClotTriever XL Catheter | Inari Medical, Inc. | 2023 |
Trace the full predicate network for K242557
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.