Class Class II
Medtronic Stedi Extra Support Guidewire (K250075)
Description
Medtronic Stedi Extra Support Guidewire by Medtronic, Inc., an FDA 510(k) cleared cardiovascular device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK250075
Clearance Date2025-06-13
Clearance TypeTraditional
Product CodeDQX
Regulation Number870.1330
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K250075
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. Medtronic Stedi Extra Support Guidewire (K250075) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K220137 | Lunderquist Extra Stiff Wire Guide | William Cook Europe Aps | 2022 |
| K181001 | Medtronic Confida Brecker Guidewire | Medtronic Core Valve, LLC | 2018 |
Trace the full predicate network for K250075
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.