# K082559: Spectranetics Cross-Pilot Turbo Elite Support Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Spectranetics Corp.
- Decided: Dec 11, 2008 after 98 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: 4 generations back to K921310 (1992). 9 ancestors in all.
1 later device descends from it; 1 cites it directly.
1 of 11 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K992051: Radifocus Optitorque, Terumo Medical Corp. (1999) Summary page 1.
- K051561: Asahi Angiographic Catheter, Asahi Intecc Co., Ltd. (2005) Summary page 1.

## Most influential descendants
- K090913: Cross-Pilot Turbo Elite Support Catheter (2009), 0 descendants of its own

## Indications for use
Cross-Pilot Turbo Elite Support Catheters are intended to guide and support Spectranetics laser catheters during access of the vasculature and provide a conduit for the delivery of saline solutions or diagnostic contrast agents.

Source page: https://510kreport.com/device/K082559
Methodology: https://510kreport.com/methodology