# K093647: Traxcess Docking Wire

- Pathway: 510(k) (Traditional)
- Applicant: MicroVention, Inc.
- Decided: Feb 24, 2010 after 91 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: 4 generations back to K953533 (1995). 4 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K080563: Runthrough NS Extension Wire, Terumo Medical Corp. (2008) Summary page 1.

## Most influential descendants
- K112219: Tapas Catheter (2011), 1 descendant of its own
- K141175: Renovocath RC120 (2014), 0 descendants of its own

## Indications for use
The Traxcess Docking Wire is intended for general intravascular use, including the neuro and peripheral vasculature. The Traxcess Docking Wire can be used with Traxcess guidewires to facilitate the placement of diagnostic or therapeutic catheters. This device is not intended for use in coronary arteries.

Source page: https://510kreport.com/device/K093647
Methodology: https://510kreport.com/methodology