# K014118: Modification to Supercross Catheter

- Pathway: 510(k) (Special)
- Applicant: Abbott Vascular, Inc.
- Decided: Jan 11, 2002 after 28 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: 1 generation back to K001856 (2001). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K001856: Supercross Catheter, Abbott Vascular, Inc. (2001) Summary page 1.

## Indications for use
The SuperCross Catheter is intended to negotiate stenotic or tortuous lesions of the iliac, femoral, popliteal, tibial and renal arteries in order to facilitate placement and positioning of other catheters. The SuperCross Catheter is not intended for use in the coronary or cerebral vasculature. The SuperCross Catheter is not intended for use to dilate lesions.

Source page: https://510kreport.com/device/K014118
Methodology: https://510kreport.com/methodology