# K090509: Foxcross .035 Pta Catheter 14 MM X 20MM X 80 CM, Model 10342-20, Foxcross .035 Pta Catheter

- Pathway: 510(k) (Special)
- Applicant: Abbott Vascular-Vascular Solutions
- Decided: Mar 20, 2009 after 22 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) FoxCross PTA Catheter: named in the summary without a submission number
- (no number) Agiltrac .035 PTA Catheter: named in the summary without a submission number

## Most influential descendants
- K111899: Armada 35/35LL Pta Catheter (2011), 0 descendants of its own

## Indications for use
The FoxCross PTA Catheter is intended for dilatation of lesions in the femoral, renal, iliac, popliteal, peroneal, and profunda arteries and native or synthetic arteriovenous dialysis fistula. This catheter is not intended for the expansion or delivery of stents.

Source page: https://510kreport.com/device/K090509
Methodology: https://510kreport.com/methodology