Class Class II
Riptide Aspiration System (K243080)
Description
Riptide Aspiration System by Micro Therapeutics, Inc. d/b/a ev3 Neurovascular, an FDA 510(k) cleared cardiovascular device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK243080
Clearance Date2024-10-29
Clearance TypeSpecial
Product CodeNRY
Regulation Number870.1250
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K243080
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. Riptide Aspiration System (K243080) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K201689 | Riptide Aspiration System | Micro Therapeutics, Inc. d/b/a ev3 ... | 2020 |
Trace the full predicate network for K243080
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.