# K090913: Cross-Pilot Turbo Elite Support Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Spectranetics Corp.
- Decided: May 4, 2009 after 33 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: 5 generations back to K921310 (1992). 10 ancestors in all.
No later device cites it as a predicate yet.
1 of 11 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082559: Spectranetics Cross-Pilot Turbo Elite Support Catheter, Spectranetics Corp. (2008) Summary page 2.

## 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 solution or diagnostic contrast agents.

Source page: https://510kreport.com/device/K090913
Methodology: https://510kreport.com/methodology