# K071336: Angiojet Xpeedior Rheolytic Thrombectomy Catheter, Model 104307

- Pathway: 510(k) (Traditional)
- Applicant: Possis Medical, Inc.
- Decided: Aug 24, 2007 after 105 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.
33 later devices descend from it; 1 cites it directly.
1 of 44 devices in its family (counting itself) has 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
- 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
- K151313: ZelanteDVT Thrombectomy Set (2015), 26 descendants of its own

## Indications for use
The AngioJet XPEEDIOR 120 Rheolytic Thrombectomy Catheter is intended for use with the AngioJet System in breaking apart and removing thrombus from: · infra-inguinal peripheral arteries > 3.0 mm in diameter, * upper extremity peripheral veins > 3.0 mm in diameter and * ileofemoral and lower extremity veins > 3.0 mm in diameter.

Source page: https://510kreport.com/device/K071336
Methodology: https://510kreport.com/methodology