# K130714: Progigy Support Catheter

- Pathway: 510(k) (Abbreviated)
- Applicant: Radius Medical, LLC
- Decided: Aug 22, 2013 after 160 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: 6 generations back to K935425 (1994). 13 ancestors in all.
4 later devices descend from it; 1 cites it directly.
1 of 18 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082337: Minnie Support Catheter, Vascular Solutions, Inc. (2009) Summary page 1.
- P860019: Scimed Ptca Dilatation Catheter, Scimed Life Systems, Inc. (1986) Summary page 1.

## Most influential descendants
- K140910: Centercross Catheter (2014), 3 descendants of its own
- 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 Prodigy Support Catheter is intended to be used in conjunction with steerable guidewires in order to access discrete regions of the arterial and or coronary vasculature. It may be used to facilitate placement and exchange of guidewires and other interventional devices.

Source page: https://510kreport.com/device/K130714
Methodology: https://510kreport.com/methodology