# K071514: Angiojet Xpeedior Rheolytic Thrombectomy Catheter, Model 104307

- Pathway: 510(k) (Traditional)
- Applicant: Possis Medical, Inc.
- Decided: Jul 31, 2007 after 57 days
- Product code: QEZ (Aspiration Thrombectomy Catheter)
- Device class: 2
- Regulation: 21 CFR 870.5150
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K901627 (1990). 10 ancestors in all.
63 later devices descend from it; 3 cite it directly.
4 of 74 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K040013: Angiojet Xpeedior 120 Catheter and Angiojet Power Pulse Spray Ancillary Kit, Possis Medical, Inc. (2004) Summary page 5.
- K052256: Angiojet Xpeedior 120 Catheter, Possis Medical, Inc. (2005) Summary page 5.
- K061951: Angiojet Xpeedior Rheolytic Thrombectomy Catheter, Model Xpeedior 120, Possis Medical, Inc. (2006) Summary page 5.

## Most influential descendants
- K072269: Angiojet Ultra DVX Thrombectomy Set, Model: 106552 (2007), 33 descendants of its own
- K090253: Angiojet Ultra DVX Thrombectomy Set, Model 106552-001, Angiojet Ultra Xpeedior Thrombectomy Set, Model 105040-001 (2009), 32 descendants of its own
- K091593: Angio Jet Ultra DVX and Xpeedior Thrombectomy Sets (2009), 31 descendants of its own
- K101406: Angiojet Solent Proxi Thrombectomy Set Model 109676-001 (2010), 30 descendants of its own
- K111182: Angiojet Solent Omni Thrombectomy Set (2011), 28 descendants of its own

## Indications for use
The AngioJet XPEEDIOR Rheolytic Thrombectomy Catheter is intended for use with the AngioJet System in breaking apart and removing thrombus from: upper and lower extremity peripheral arteries > 3.0 mm in diameter and upper extremity and infrainguinal lower extremity peripheral veins > 3.0 mm in diameter.

Source page: https://510kreport.com/device/K071514
Methodology: https://510kreport.com/methodology