510(k) · Cleared
ClearedAkonya Eliminator Mechanical Thrombectomy Device, Model EL 10060060
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Idev Technologies, Inc. · MCW Catheter, Peripheral, Atherectomy
Cleared on Sep 16, 2003 as substantially equivalent to K970080 (Arrow Intl., Inc., 1997) and 1 other predicate after a 209-day review. Its family tree reaches back 1 generation to 1997. 1 later device descends from it.
- Decided
- Sep 16, 2003
- Review
- 209 days
- Class
- Class II
- Product code
- MCW
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 1 generation to K970080 (1997). 2 ancestors in all. 1 later device descends from it, 1 citing it directly.
- Root · 1 generation backK970080 Arrow-Trerotola PTD CatheterArrow Intl., Inc. · 1997
- This deviceK030504 Akonya Eliminator Mechanical Thrombectomy Device, Model EL 10060060Idev Technologies, Inc. · 2003
- Descendant · cites it directly · 0 of its ownK041374 Akonya Eliminator Mechanical Thrombectomy Device, Model EL10060060Idev Technologies, Inc. · 2005
Most influential descendants
Showing 1 of 1 · See all- K041374Akonya Eliminator Mechanical Thrombectomy Device, Model EL10060060Idev Technologies, Inc. · 2005 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K970080 | Arrow-Trerotola PTD Catheter | Arrow Intl., Inc. | 1997 | — |
| 0 (this device) | K030504 | Akonya Eliminator Mechanical Thrombectomy Device, Model EL 10060060 | Idev Technologies, Inc. | 2003 | — |
| +1 | K041374 | Akonya Eliminator Mechanical Thrombectomy Device, Model EL10060060 | Idev Technologies, Inc. | 2005 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1999 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2005 | 1 | 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.
Planning a device in MCW? 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 MCW device
- #1 K233668 Auryon Atherectomy Catheter 1.5 mm XL…score 17.6 · 18 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
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 |
|---|---|---|---|
| * | K970080 | Arrow-Trerotola PTD CatheterSummary page 1…Catheter, Peripheral, Atherectomy (2 1 CFR 870.4875) Product Code: MCW Predicate Device: Arrow-Trerotola TM Percutaneous Thrombolytic Device (PTD) (K970080, K990829) Device Description: The AKonya EliminatorTMMechanical Thrombectomy Device is comprised of three d… | 1997 |
| * | K990829 | Arrow-Trerotola Percutaneous Thrombolytic Device or PTD, Models PT-45509 (Catheter Kit…Summary page 1…, Atherectomy (2 1 CFR 870.4875) Product Code: MCW Predicate Device: Arrow-Trerotola TM Percutaneous Thrombolytic Device (PTD) (K970080, K990829) Device Description: The AKonya EliminatorTMMechanical Thrombectomy Device is comprised of three discrete elements: An o… | 1999 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K041374 | Akonya Eliminator Mechanical Thrombectomy Device, Model EL10060060 | 2005 | 0 |
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
How does its category compare?
All MCW devicesMCW Catheter, Peripheral, Atherectomy: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · MCW
3in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · MCW
46in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · MCW
2in 2024
Class I (4 since 2007) Class II/III not classified
Adverse event reports per year · MCW
677in 2025
MAUDE reports naming product code MCW, 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 | 5 | 43 | 2 | 50 |
| 2008 | 6 | 33 | 1 | 115 |
| 2009 | 8 | 27 | 3 | 105 |
| 2010 | 6 | 30 | 1 | 167 |
| 2011 | 6 | 39 | 0 | 204 |
| 2012 | 5 | 29 | 0 | 194 |
| 2013 | 5 | 30 | 0 | 134 |
| 2014 | 7 | 117 | 0 | 210 |
| 2015 | 6 | 30 | 0 | 377 |
| 2016 | 5 | 60 | 2 | 409 |
| 2017 | 7 | 91 | 2 | 415 |
| 2018 | 8 | 103 | 0 | 537 |
| 2019 | 3 | 112 | 0 | 618 |
| 2020 | 2 | — | 0 | 631 |
| 2021 | 6 | 119 | 2 (2) | 734 |
| 2022 | 6 | 69 | 2 (2) | 566 |
| 2023 | 4 | 104 | 1 | 574 |
| 2024 | 3 | 41 | 2 | 677 |
| 2025 | 3 | 46 | 0 | 677 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
The AK6nya EliminatorTMMechanical Thrombectomy Device is indicated for use in the mechanical declotting of synthetic dialysis grafts.
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/K030504 · printed Nov 6, 2026
Cite this page
510(k) Report. “K030504: Akonya Eliminator Mechanical Thrombectomy Device, Model EL 10060060.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K030504
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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