# K080925: Fox Plus Pta Catheter

- Pathway: 510(k) (Special)
- Applicant: Abbott Vascular, Inc.
- Decided: Apr 28, 2008 after 26 days
- Product code: LIT (Catheter, Angioplasty, Peripheral, Transluminal)
- 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: 4 generations back to K000101 (2000). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K080264: Modification to: Fox Plus Pta Catheter, Abbott Vascular-Vascular Solutions (2008) Summary page 1.

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

Source page: https://510kreport.com/device/K080925
Methodology: https://510kreport.com/methodology