Class Class II
Artix BG (K223000)
Description
Artix BG by Inari Medical, an FDA 510(k) cleared cardiovascular device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK223000
Clearance Date2023-01-11
Clearance TypeTraditional
Product CodeQEW
Regulation Number870.5150
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K223000
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. Artix BG (K223000) cites 2 predicate devices and is itself cited by 1 later device.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K221846 | Artix Ballon Guiding Sheath | Inari Medical | 2022 |
| K212632 | ClotTriever Thrombectomy System | Inari Medical, Inc. | 2021 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K230912 | Artix BG | Inari Medical | 2023 |
Trace the full predicate network for K223000
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.