# K110241: Endologix Guidewire

- Pathway: 510(k) (Special)
- Applicant: Techdevice Corporation
- Decided: Feb 25, 2011 after 29 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
Longest line of descent: 2 generations back to K013723 (2002). 6 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K053251: Techdevice Guidewire, Techdevice Corporation (2006) Summary page 1.
- K053258: Eub-6500 Diagnostic Ultrasound Scanner, Hitachi Medical Corp. (2005) Summary page 2.

## Most influential descendants
- K152177: SonoStik IV Guide Wire Introducer (2015), 1 descendant of its own
- K243061: SonoStik Guide Wire Introducer (2024), 0 descendants of its own

## Indications for use
The Guidewire facilitates placement and exchange of catheters and other instruments in the peripheral vasculature. This guidewire is not intended for use in the coronary arteries or neurovasculature.

Source page: https://510kreport.com/device/K110241
Methodology: https://510kreport.com/methodology