# K051519: Fox SV Pta Catheter (82XXX Series).   Fox Plus Pta Catheter (12XXX Series)

- Pathway: 510(k) (Special)
- Applicant: Abbott Laboratories (Perclose, Inc.)
- Decided: Jun 21, 2005 after 13 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: 3 generations back to K000101 (2000). 5 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K040954: Fox Plus Pta Catheter, Abbott Laboratories, Inc. (2004) Summary page 1.

## Most influential descendants
- K062843: Fox SV Pta Catheter (2006), 1 descendant of its own
- K072824: Fox SV Pta Catheter (2007), 0 descendants of its own

## Indications for use
The Fox SV 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/K051519
Methodology: https://510kreport.com/methodology