# K140910: Centercross Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Roxwood Medical, Inc.
- Decided: Nov 19, 2014 after 224 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K001992 (2000). 47 ancestors in all.
3 later devices descend from it; 1 cites it directly.
5 of 51 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K121763: Multicross Support Catheter, Roxwood Medical, Inc. (2012) Summary page 5.
- K130714: Progigy Support Catheter, Radius Medical, LLC (2013) Summary page 5.

## Most influential descendants
- K152456: CenterCross Ultra Catheter (2016), 2 descendants of its own
- K160681: CenterCross Ultra Catheter (2016), 1 descendant of its own
- K170403: CenterCross Ultra LV Catheter (2017), 0 descendants of its own

## Indications for use
The CenterCross Catheter is intended to be used in conjunction with steerable guidewires to access discrete regions of the coronary and peripheral vasculature. It may be used to facilitate placement and exchange of guidewires and other interventional devices.

Source page: https://510kreport.com/device/K140910
Methodology: https://510kreport.com/methodology