# K013473: XTD Thrombectomy Catheter, XX CM, Model# CT000500X; XTD Control Console, Model # CT0006001; XTD Collection Bottle, Model

- Pathway: 510(k) (Traditional)
- Applicant: Xtrak Medical, Inc.
- Decided: Mar 6, 2002 after 139 days
- Product code: MCW (Catheter, Peripheral, Atherectomy)
- Device class: 2
- Regulation: 21 CFR 870.4875
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K901627 (1990). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K960970: Possis Angiojet Rapid Thrombectomy  Catheter System, F105 Catheter,Model 3030C,LF140 Catheter,Model 3040C,Pump Set 3020P, Possis Medical, Inc. (1996) Summary page 1.
- K970080: Arrow-Trerotola PTD Catheter, Arrow Intl., Inc. (1997) Summary page 1.

## Most influential descendants
- K021641: XTD Thrombectomy Catheter, XX CM (2002), 0 descendants of its own

## Indications for use
For breaking apart and removing thrombus from hemodialysis access grafts.

Source page: https://510kreport.com/device/K013473
Methodology: https://510kreport.com/methodology