510(k) Report

510(k) · Cleared

Cleared

Pounce XL Thrombectomy System (PTS-1011-7F135)

K241362510(k) TraditionalCleared Sep 11, 2024120-day reviewClass II21 CFR 870.5150

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Surmodics,Inc. · QEW Peripheral Mechanical Thrombectomy With Aspiration

Cleared on Sep 11, 2024 as substantially equivalent to K220501 (Surmodics,Inc., 2022) and 1 other predicate after a 120-day review. Its family tree reaches back 7 generations to 1997.

Decided
Sep 11, 2024
Review
120 days
Class
Class II
Product code
QEW
Recalls
None
Predicates
2

Its longest line of descent runs back 7 generations to K970657 (1997). 11 ancestors in all, the oldest K892410 (1989). No later device cites it as a predicate yet.

  1. Root · 7 generations backK970657 Lmi Thrombectomy CatheterLucas Medical, Inc. · 1997
  2. 6 generations backK070403 Pronto .035 Extraction CatheterVascular Solutions, Inc. · 2007
  3. 5 generations backK110315 Nexgen Peripheral Mechanical Retrieval DeviceNexgen Medical Systems, Inc. · 2011
  4. 4 generations backK192814 Pounce Thrombus Retrieval SystemSurmodics,Inc. · 2020
  5. 3 generations backK211492 Pounce Thrombectomy SystemSurmodics,Inc. · 2021
  6. 2 generations backK220501 Pounce Thrombectomy SystemSurmodics,Inc. · 2022
  7. 1 generation backK231022 Pounce™ Thrombectomy SystemSurmodics,Inc. · 2023
  8. This deviceK241362 Pounce XL Thrombectomy System (PTS-1011-7F135)Surmodics,Inc. · 2024
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K970657Lmi Thrombectomy CatheterLucas Medical, Inc.1997—
−6K070403Pronto .035 Extraction CatheterVascular Solutions, Inc.2007—
−5K110315Nexgen Peripheral Mechanical Retrieval DeviceNexgen Medical Systems, Inc.2011—
−4K192814Pounce Thrombus Retrieval SystemSurmodics,Inc.2020—
−3K211492Pounce Thrombectomy SystemSurmodics,Inc.2021—
−2K220501Pounce Thrombectomy SystemSurmodics,Inc.2022—
−1K231022Pounce™ Thrombectomy SystemSurmodics,Inc.2023—
0 (this device)K241362Pounce XL Thrombectomy System (PTS-1011-7F135)Surmodics,Inc.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198910
200010
200510
200910
FIG. 1 — Lineage of K241362, 1997–2024Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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 QEW? 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 QEW device

  1. #1 K213402 Triever24, Triever20score 28.6 · 5 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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.

TypeNumberDeviceApplicantDecidedRecalls
*K220501Pounce Thrombectomy System
Summary page 5
…7F135) Common / Usual Name: Thrombectomy Catheter Classification: Class II Product Code: QEW 21 CFR 870.5150 Predicate Devices: K220501 Pounce™ Thrombectomy System K231022 Pounce™ LP Thrombectomy System…
Surmodics,Inc.2022—
*K231022Pounce™ Thrombectomy System
Summary page 5
…fication: Class II Product Code: QEW 21 CFR 870.5150 Predicate Devices: K220501 Pounce™ Thrombectomy System K231022 Pounce™ LP Thrombectomy System…
Surmodics,Inc.2023—

Also cleared against K220501: 1 other device →

What descends from it?

No later submission names this one as a predicate yet.

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?

  • The line of descent spans 27 years and passes through 4 companies; a new generation was cleared every 1.3 years on median.
  • 2 of the 11 ancestors have a recall of any class.
  • 1 other device also cites its predicate K220501.

How does its category compare?

All QEW devices

QEW Peripheral Mechanical Thrombectomy With Aspiration: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.

FDA decisions per year · QEW

14in 2025

2008: 22009: 22012: 12013: 22014: 22015: 42016: 42017: 22018: 142019: 82020: 162021: 112022: 122023: 232024: 142025: 142026 (partial year): 10
2007high 23 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QEW

58in 2025

2015: 88 days median2016: 63 days median2018: 61 days median2019: 51 days median2020: 105 days median2021: 60 days median2022: 140 days median2023: 102 days median2024: 65 days median2025: 58 days median2026 (partial year): 74 days median
2007high 140 (2022) · low 51 (2019)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · QEW

7in 2022

2022: 7, 7 Class I
2007high 7 (2022) · low 0 (2007)2026

Class I (7 since 2007) Class II/III not classified

Adverse event reports per year · QEW

207in 2025

2019: 332020: 1972021: 3222022: 1252023: 1652024: 1622025: 207
2007high 322 (2021) · low 0 (2007)2025

MAUDE reports naming product code QEW, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20082—00
20092—00
20100—00
20110—00
20121—00
20132—00
20142—00
201548800
201646300
20172—00
2018146100
2019851033
2020161050197
202111600322
2022121407 (7)125
2023231020165
202414650162
202514580207
202610740—

What is it indicated for?

The Pounce Thrombectomy System is intended for the non-surgical removal of thrombi and emboli from the peripheral arterial vasculature.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K241362: Pounce XL Thrombectomy System (PTS-1011-7F135).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K241362

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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