# K010511: Modification to: Agility Steerable Guidewires

- Pathway: 510(k) (Special)
- Applicant: Cordis Neurovascular, Inc.
- Decided: Mar 1, 2001 after 8 days
- Product code: DQX (Wire, Guide, Catheter)
- Device class: 2
- Regulation: 21 CFR 870.1330
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 2 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K100351: Neuroscout Steerable Guidewire (2010), 3 descendants of its own
- K121776: Agility Steerable Guidewire Neuroscout Steerable Gudiewire (2012), 1 descendant of its own
- K151825: Viradius Neurowire (2015), 0 descendants of its own
- K133625: Agility 10 Standard & Soft 0.01IN. X 195CM, Agility 14 Standard & Soft 0.014IN X 205CM & XL 350CM, Agility 16 Standard & (2014), 0 descendants of its own

Source page: https://510kreport.com/device/K010511
Methodology: https://510kreport.com/methodology