510(k) · Cleared
ClearedAngiojet Ultra Avx Thrombectomy Set, Model 105039
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Possis Medical, Inc. · QEZ Aspiration Thrombectomy Catheter
Cleared on Jan 24, 2008 as substantially equivalent to K960970 (Possis Medical, Inc., 1996) and 2 other predicates after a 48-day review. Its family tree reaches back 3 generations to 1990. 1 of the 40 devices in its family, counting itself, has a Class I recall. 35 later devices descend from it.
- Decided
- Jan 24, 2008
- Review
- 48 days
- Class
- Class II
- Product code
- QEZ
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 3 generations to K901627 (1990). 4 ancestors in all. 35 later devices descend from it, 1 citing it directly. 1 of the 40 devices in this family, counting this one, has a Class I recall.
- Root · 3 generations backK901627 Arterial Embolectomy CatheterApplied Vascular Devices, Inc. · 1990 · Recalled
- 2 generations backK960970 Possis Angiojet Rapid Thrombectomy Catheter System, F105…Possis Medical, Inc. · 1996
- 1 generation backK972610 Possis Angiojet Rapid Thombectomy Catheters--F105 Catheter Model…Possis Medical, Inc. · 2000
- This deviceK073441 Angiojet Ultra Avx Thrombectomy Set, Model 105039Possis Medical, Inc. · 2008
- Descendant · cites it directly · 34 of its ownK082382 Angiojet Ultra Avx Thrombectomy Set, Model 105039Possis Medical, Inc. · 2008
- Descendant · 2 generations on · 32 of its ownK090253 Angiojet Ultra DVX Thrombectomy Set, Model 106552-001, Angiojet…Possis Medical, Inc. · 2009
- Descendant · 3 generations on · 31 of its ownK091593 Angio Jet Ultra DVX and Xpeedior Thrombectomy SetsPossis Medical, Inc. · 2009
- Descendant · 4 generations on · 30 of its ownK101406 Angiojet Solent Proxi Thrombectomy Set Model 109676-001Medrad Interventional/Possis · 2010
- Descendant · 4 generations on · 28 of its ownK111182 Angiojet Solent Omni Thrombectomy SetMedrad, Inc. · 2011 · Recalled
Showing 5 of 35 descendants. See all descendants
Descendants cleared per year
Class I recalls in this family
- K223210 ClotTriever XL Catheter10 generations on · 2023
Most influential descendants
Showing 5 of 35 · See all- K082382Angiojet Ultra Avx Thrombectomy Set, Model 105039Possis Medical, Inc. · 2008 · cites it directly34descendants
- K090253Angiojet Ultra DVX Thrombectomy Set, Model 106552-001, Angiojet Ultra Xpeedior…Possis Medical, Inc. · 2009 · 2 generations on32descendants
- K091593Angio Jet Ultra DVX and Xpeedior Thrombectomy SetsPossis Medical, Inc. · 2009 · 3 generations on31descendants
- K101406Angiojet Solent Proxi Thrombectomy Set Model 109676-001Medrad Interventional/Possis · 2010 · 4 generations on30descendants
- K111182Angiojet Solent Omni Thrombectomy SetMedrad, Inc. · 2011 · 4 generations on28descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K901627 | Arterial Embolectomy Catheter | Applied Vascular Devices, Inc. | 1990 | 1 |
| −2 | K960970 | Possis Angiojet Rapid Thrombectomy Catheter System, F105 Catheter,Model… | Possis Medical, Inc. | 1996 | — |
| −1 | K972610 | Possis Angiojet Rapid Thombectomy Catheters--F105 Catheter Model 3030C, LF140… | Possis Medical, Inc. | 2000 | — |
| 0 (this device) | K073441 | Angiojet Ultra Avx Thrombectomy Set, Model 105039 | Possis Medical, Inc. | 2008 | — |
| +1 | K082382 | Angiojet Ultra Avx Thrombectomy Set, Model 105039 | Possis Medical, Inc. | 2008 | — |
| +2 | K090253 | Angiojet Ultra DVX Thrombectomy Set, Model 106552-001, Angiojet Ultra Xpeedior… | Possis Medical, Inc. | 2009 | — |
| +3 | K091593 | Angio Jet Ultra DVX and Xpeedior Thrombectomy Sets | Possis Medical, Inc. | 2009 | — |
| +4 | K101406 | Angiojet Solent Proxi Thrombectomy Set Model 109676-001 | Medrad Interventional/Possis | 2010 | — |
| +4 | K111182 | Angiojet Solent Omni Thrombectomy Set | Medrad, Inc. | 2011 | 1 |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2000 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2008 | 1 | 0 |
| 2009 | 2 | 0 |
| 2010 | 1 | 0 |
| 2011 | 2 | 0 |
| 2012 | 1 | 0 |
| 2014 | 1 | 0 |
| 2015 | 1 | 0 |
| 2020 | 2 | 0 |
| 2021 | 3 | 0 |
| 2022 | 2 | 0 |
| 2023 | 9 | 1 |
| 2024 | 3 | 0 |
| 2025 | 4 | 0 |
| 2026 | 3 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
1 device in this family has a Class I recall. A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new QEZ device
- #1 K253925 Aventus Thrombectomy Systemscore 17.9 · 5 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (3)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K960970 | Possis Angiojet Rapid Thrombectomy Catheter System, F105 Catheter,Model 3030C,LF140…Summary page 5…7 Email: [email protected] December 6, 2007 AngioJet® Ultra AVX® Thrombectomy Set 870.5150 DXE The subject devices are equivalent to the following devices: e K960970 AngioJet Rapid Thrombectomy System — Pump Set e K972610 AngioJet LF140 Catheter o K993564 AngioJet XPEEDIOR® 60 Rheolytic Thrombe… | 1996 |
| * | K972610 | Possis Angiojet Rapid Thombectomy Catheters--F105 Catheter Model 3030C, LF140 Catheter…Summary page 5…gioJet® Ultra AVX® Thrombectomy Set 870.5150 DXE The subject devices are equivalent to the following devices: e K960970 AngioJet Rapid Thrombectomy System — Pump Set e K972610 AngioJet LF140 Catheter o K993564 AngioJet XPEEDIOR® 60 Rheolytic Thrombectomy Catheter e KO071342 AngioJet XPEEDIOR® Thrombectom… | 2000 |
| * | K993564 | Possis Angiojet X-Stream Rheolytic Thrombectomy Catheter, Model 103587-002Summary page 5…t 870.5150 DXE The subject devices are equivalent to the following devices: e K960970 AngioJet Rapid Thrombectomy System — Pump Set e K972610 AngioJet LF140 Catheter o K993564 AngioJet XPEEDIOR® 60 Rheolytic Thrombectomy Catheter e KO071342 AngioJet XPEEDIOR® Thrombectomy Set (reference device-design onl… | 2000 |
| † | K071342 | Angiojet Ultra Xpeedior Thrombectomy Set, Model 105040, 105042, 106552, 105043, 105041… | 2007 |
| † | K072269 | Angiojet Ultra DVX Thrombectomy Set, Model: 106552 | 2007 |
| † | K072769 | Angiojet Ultra; Xmi (105041), XVG (105042) and Spiroflex (106553) Thrombectomy Sets | 2007 |
What descends from it? (35)
See all 351 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K082382 | Angiojet Ultra Avx Thrombectomy Set, Model 105039 | 2008 | 34 |
Has anything in its family been recalled? (1 Class I)
No FDA recall names this device.
Relatives with a Class I recall
Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.
- K223210ClotTriever XL CatheterInari Medical, Inc. · 2023 · 10 generations on · ◆ in the 2023 descendants bar of FIG. 11 Class I recall
What does this lineage say?
- The line of descent spans 18 years and passes through 2 companies; a new generation was cleared every 6.1 years on median.
- 1 of the 4 ancestors has a recall of any class.
- Of its descendants, K082382 (Possis Medical, Inc., 2008) has gone furthest, with 34 descendants of its own.
- 6 other devices also cite its predicate K960970.
How does its category compare?
All QEZ devicesQEZ Aspiration Thrombectomy Catheter: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.
FDA decisions per year · QEZ
5in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · QEZ
108in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · QEZ
No recall names QEZ since 2007.
Adverse event reports per year · QEZ
21in 2025
MAUDE reports naming product code QEZ, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 11 | 79 | 0 | 0 |
| 2008 | 6 | 72 | 0 | 0 |
| 2009 | 4 | 83 | 0 | 0 |
| 2010 | 3 | 33 | 0 | 0 |
| 2011 | 7 | 118 | 0 | 0 |
| 2012 | 5 | 90 | 0 | 0 |
| 2013 | 4 | 144 | 0 | 0 |
| 2014 | 1 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 1 | — | 0 | 0 |
| 2017 | 3 | 112 | 0 | 0 |
| 2018 | 1 | — | 0 | 0 |
| 2019 | 3 | 94 | 0 | 0 |
| 2020 | 3 | 120 | 0 | 0 |
| 2021 | 3 | 53 | 0 | 2 |
| 2022 | 2 | — | 0 | 18 |
| 2023 | 1 | — | 0 | 14 |
| 2024 | 1 | — | 0 | 17 |
| 2025 | 5 | 108 | 0 | 21 |
| 2026 | 6 | 98 | 0 | — |
What is it indicated for?
The AngioJet Ultra AVX Thrombectomy Set is intended for use with the AngioJet Ultra System in breaking apart and removing thrombus from A-V access conduits > 3.0mm in diameter.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K073441 · printed Nov 6, 2026
Cite this page
510(k) Report. “K073441: Angiojet Ultra Avx Thrombectomy Set, Model 105039.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K073441
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026