510(k) Report

510(k) · Cleared

Recalled · Class I · 2020

Penumbra System (Penumbra JET 7 Reperfusion Catheter with Xtra Flex Technology; Penumbra JET 7MAX)

K202251510(k) SpecialCleared Aug 31, 202021-day reviewClass II21 CFR 870.1250Recalls 4 (4 Class I)

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

Penumbra, Inc. · NRY Catheter, Thrombus Retriever

Cleared on Aug 31, 2020 as substantially equivalent to K190010 (Penumbra, Inc., 2019) and 1 other predicate after a 21-day review. Its family tree reaches back 13 generations to 2001. 4 of the 19 devices in its family, counting itself, have a Class I recall. It has been recalled 4 times, including 4 Class I recalls.

Decided
Aug 31, 2020
Review
21 days
Class
Class II
Product code
NRY
Recalls
4 (4 Class I)
Predicates
2

Its longest line of descent runs back 13 generations to K003410 (2001). 18 ancestors in all, the oldest K003086 (2001). No later device cites it as a predicate yet. 4 of the 19 devices in this family, counting this one, have a Class I recall.

Other ancestors, by year cleared 2017: 1 other ancestor, 1 with a Class I recall12012: 1 other ancestor2014: 1 other ancestor2009: 1 other ancestor2001: 1 other ancestorK003410 · Concentric Retriever, Model 90030 · Concentric Medical, Inc. · 2001 · recalledK030476 · Modified Concentric Retriever, Model 90037 · Concentric Medical, Inc. · 2003 · recalledK033736 · Merci Retriever, Models 90065, 90066 · Concentric Medical, Inc. · 2004K072718 · Penumbra System · Penumbra, Inc. · 2007 · recalledK100769 · Penumbra System Separator Flex (026,032,041,054), Models PSF026, PSF032, PSF041, PSF054 · Penumbra, Inc. · 2010K113163 · Penumbra System Max · Penumbra, Inc. · 2011K142458 · Penumbra System ACE · Penumbra, Inc. · 2015K152541 · Penumbra System ACE 64 and ACE 68 Reperfusion Catheters · Penumbra, Inc. · 2016×2: 2 generations cleared close together, K160449 (2016), K161640 (2016) K173761 · Penumbra System Reperfusion Catheter JET 7 · Penumbra, Inc. · 2018K190010 · Penumbra System Reperfusion Catheter JET 7 · Penumbra, Inc. · 2019 · Class I recallK191946 · Penumbra System Penumbra JET 7X · Penumbra, Inc. · 2020 · Class I recall20002005201020152020
Other ancestors, by generation 3 generations back: 1 other ancestor, 1 with a Class I recall15 generations back: 1 other ancestor7 generations back: 2 other ancestors8 generations back: 1 other ancestor K191946 · Penumbra System Penumbra JET 7X · Penumbra, Inc. · 2020 · Class I recallK190010 · Penumbra System Reperfusion Catheter JET 7 · Penumbra, Inc. · 2019 · Class I recallK173761 · Penumbra System Reperfusion Catheter JET 7 · Penumbra, Inc. · 2018K161640 · Penumbra System ACE 68 Reperfusion Catheter · Penumbra, Inc. · 2016K160449 · Penumbra System, Penumbra Pump MAX · Penumbra, Inc. · 2016K152541 · Penumbra System ACE 64 and ACE 68 Reperfusion Catheters · Penumbra, Inc. · 2016K142458 · Penumbra System ACE · Penumbra, Inc. · 2015K113163 · Penumbra System Max · Penumbra, Inc. · 2011K100769 · Penumbra System Separator Flex (026,032,041,054), Models PSF026, PSF032, PSF041, PSF054 · Penumbra, Inc. · 2010K072718 · Penumbra System · Penumbra, Inc. · 2007 · recalledK033736 · Merci Retriever, Models 90065, 90066 · Concentric Medical, Inc. · 2004K030476 · Modified Concentric Retriever, Model 90037 · Concentric Medical, Inc. · 2003 · recalledK003410 · Concentric Retriever, Model 90030 · Concentric Medical, Inc. · 2001 · recalled−10−50
  1. Root · 13 generations backK003410 Concentric Retriever, Model 90030Concentric Medical, Inc. · 2001 · Recalled
  2. 9 generations between
  3. 3 generations backK173761 Penumbra System Reperfusion Catheter JET 7Penumbra, Inc. · 2018
  4. 2 generations backK190010 Penumbra System Reperfusion Catheter JET 7Penumbra, Inc. · 2019 · Recalled (Class I)
  5. 1 generation backK191946 Penumbra System Penumbra JET 7XPenumbra, Inc. · 2020 · Recalled (Class I)
  6. This deviceK202251 Penumbra System (Penumbra JET 7 Reperfusion Catheter with Xtra Flex…Penumbra, Inc. · 2020
Show all 13 generations
  1. Root · 13 generations backK003410 Concentric Retriever, Model 90030Concentric Medical, Inc. · 2001 · Recalled
  2. 12 generations backK030476 Modified Concentric Retriever, Model 90037Concentric Medical, Inc. · 2003 · Recalled
  3. 11 generations backK033736 Merci Retriever, Models 90065, 90066Concentric Medical, Inc. · 2004
  4. 10 generations backK072718 Penumbra SystemPenumbra, Inc. · 2007 · Recalled
  5. 9 generations backK100769 Penumbra System Separator Flex (026,032,041,054), Models PSF026…Penumbra, Inc. · 2010
  6. 8 generations backK113163 Penumbra System MaxPenumbra, Inc. · 2011
  7. 7 generations backK142458 Penumbra System ACEPenumbra, Inc. · 2015
  8. 6 generations backK152541 Penumbra System ACE 64 and ACE 68 Reperfusion CathetersPenumbra, Inc. · 2016
  9. 5 generations backK160449 Penumbra System, Penumbra Pump MAXPenumbra, Inc. · 2016
  10. 4 generations backK161640 Penumbra System ACE 68 Reperfusion CatheterPenumbra, Inc. · 2016
  11. 3 generations backK173761 Penumbra System Reperfusion Catheter JET 7Penumbra, Inc. · 2018
  12. 2 generations backK190010 Penumbra System Reperfusion Catheter JET 7Penumbra, Inc. · 2019 · Recalled (Class I)
  13. 1 generation backK191946 Penumbra System Penumbra JET 7XPenumbra, Inc. · 2020 · Recalled (Class I)
  14. This deviceK202251 Penumbra System (Penumbra JET 7 Reperfusion Catheter with Xtra Flex…Penumbra, Inc. · 2020

Class I recalls in this family

  • K191946 Penumbra System Penumbra JET 7Xdirect predicate · 2020
  • K190010 Penumbra System Reperfusion Catheter JET 7direct predicate · 2019
  • K162901 Penumbra 3D Revascularization Device3 generations back · 2017
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−13K003410Concentric Retriever, Model 90030Concentric Medical, Inc.20011
−12K030476Modified Concentric Retriever, Model 90037Concentric Medical, Inc.20032
−11K033736Merci Retriever, Models 90065, 90066Concentric Medical, Inc.2004—
−10K072718Penumbra SystemPenumbra, Inc.20071
−9K100769Penumbra System Separator Flex (026,032,041,054), Models PSF026, PSF032…Penumbra, Inc.2010—
−8K113163Penumbra System MaxPenumbra, Inc.2011—
−7K142458Penumbra System ACEPenumbra, Inc.2015—
−6K152541Penumbra System ACE 64 and ACE 68 Reperfusion CathetersPenumbra, Inc.2016—
−5K160449Penumbra System, Penumbra Pump MAXPenumbra, Inc.2016—
−4K161640Penumbra System ACE 68 Reperfusion CatheterPenumbra, Inc.2016—
−3K173761Penumbra System Reperfusion Catheter JET 7Penumbra, Inc.2018—
−2K190010Penumbra System Reperfusion Catheter JET 7Penumbra, Inc.2019Class I
−1K191946Penumbra System Penumbra JET 7XPenumbra, Inc.2020Class I
0 (this device)K202251Penumbra System (Penumbra JET 7 Reperfusion Catheter with Xtra Flex…Penumbra, Inc.2020—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200110
200910
201210
201410
201711
FIG. 1 — Lineage of K202251, 2001–2020Source: 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.

4 devices in this family have 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 NRY device

  1. #1 K232971 APRO 55 Catheter and Alembic Aspiration Tubingscore 18.6 · 10 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
*K190010Penumbra System Reperfusion Catheter JET 7
Summary page 4
…ation Number: 21 CFR 870.1250 Product Code: NRY (Catheter, Thrombus Removal) 1.3. Predicate Device Information Penumbra System® Reperfusion Catheter JET™ 7 (K190010) Penumbra System® [JET™ 7 Reperfusion Catheter with MAX Delivery Device (JET™ 7MAX)] (K191946). 1.4. Device Descrip…
Penumbra, Inc.2019Class I
*K191946Penumbra System Penumbra JET 7X
Summary page 4
…formation Penumbra System® Reperfusion Catheter JET™ 7 (K190010) Penumbra System® [JET™ 7 Reperfusion Catheter with MAX Delivery Device (JET™ 7MAX)] (K191946). 1.4. Device Description The Penumbra System Reperfusion Catheter Penumbra JET 7 with Xtra Flex technology (JET 7…
Penumbra, Inc.2020Class I

Also cleared against K190010: 1 other device →

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (4 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Dec 15, 2020Class IZ-0848-2021Process designThe catheter may become susceptible to distal tip damage during use. Distal tip damage in conjunction with pressurization of contrast injection may result in potential vessel damage, and subsequent patient injury or death.
Dec 15, 2020Class IZ-0851-2021Process designThe catheter may become susceptible to distal tip damage during use. Distal tip damage in conjunction with pressurization of contrast injection may result in potential vessel damage, and subsequent patient injury or death.
Dec 15, 2020Class IZ-0849-2021Process designThe catheter may become susceptible to distal tip damage during use. Distal tip damage in conjunction with pressurization of contrast injection may result in potential vessel damage, and subsequent patient injury or death.
Dec 15, 2020Class IZ-0850-2021Process designThe catheter may become susceptible to distal tip damage during use. Distal tip damage in conjunction with pressurization of contrast injection may result in potential vessel damage, and subsequent patient injury or death.

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.

  • K191946Penumbra System Penumbra JET 7XPenumbra, Inc. · 2020 · Direct predicate · ◆ on the line of descent in FIG. 14 Class I recalls
  • K190010Penumbra System Reperfusion Catheter JET 7Penumbra, Inc. · 2019 · Direct predicate · ◆ on the line of descent in FIG. 14 Class I recalls
  • K162901Penumbra 3D Revascularization DevicePenumbra, Inc. · 2017 · 3 generations back · ◆ in the 2017 ancestors bar of FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 19 years and passes through 2 companies; a new generation was cleared every 1.4 years on median.
  • 6 of the 18 ancestors have a recall of any class; 3 have a Class I recall.
  • 1 other device also cites its predicate K190010.

How does its category compare?

All NRY devices

NRY Catheter, Thrombus Retriever: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · NRY

15in 2025

2007: 52008: 22009: 22010: 12011: 22012: 42014: 42015: 62016: 52017: 32018: 112019: 72020: 62021: 92022: 32023: 82024: 82025: 152026 (partial year): 14
2007high 15 (2025) · low 0 (2013)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NRY

129in 2025

2007: 94 days median2012: 90 days median2014: 140 days median2015: 128 days median2016: 75 days median2017: 185 days median2018: 156 days median2019: 89 days median2020: 125 days median2021: 80 days median2022: 129 days median2023: 112 days median2024: 165 days median2025: 129 days median2026 (partial year): 147 days median
2007high 185 (2017) · low 75 (2016)2026

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

Recalls per year · NRY

4in 2020

2010: 12013: 12017: 42020: 4, 4 Class I2026 (partial year): 2
2007high 4 (2017) · low 0 (2007)2026

Class I (4 since 2007) Class II/III not classified

Adverse event reports per year · NRY

565in 2025

2007: 132008: 182009: 572010: 2892011: 2632012: 3662013: 4052014: 4282015: 5982016: 4972017: 4322018: 4152019: 6502020: 7032021: 6882022: 5492023: 7112024: 6412025: 565
2007high 711 (2023) · low 13 (2007)2025

MAUDE reports naming product code NRY, 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
2007594013
20082—018
20092—057
20101—1289
20112—0263
20124900366
20130—1405
201441400428
201561280598
20165750497
201731854432
2018111560415
20197890650
202061254 (4)703
20219800688
202231290549
202381120711
202481650641
2025151290565
2026141472—

What is it indicated for?

Penumbra Reperfusion Catheters and Separators As part of the Penumbra System, the Reperfusion Catheters and Separators are indicated for use in the revascularization of patients with acute ischemic stroke secondary to intracranial large vessel occlusive disease (within the internal carotid, middle cerebral – M1 and M2 segments, basilar, and vertebral arteries) within 8 hours of symptom onset. Patients who are ineligible for intravenous tissue plasminogen…

Read the full statement (195 words)

Penumbra Reperfusion Catheters and Separators

As part of the Penumbra System, the Reperfusion Catheters and Separators are indicated for use in the revascularization of patients with acute ischemic stroke secondary to intracranial large vessel occlusive disease (within the internal carotid, middle cerebral – M1 and M2 segments, basilar, and vertebral arteries) within 8 hours of symptom onset. Patients who are ineligible for intravenous tissue plasminogen activator (IV t-PA) or who fail IV t-PA therapy are candidates for treatment.

Penumbra 3D Revascularization Device

As part of the Penumbra System, the Penumbra 3D Revascularization Device is indicated for use in the revascularization of patients with acute ischemic stroke secondary to intracranial large vessel occlusive disease (within the internal carotid, middle cerebral – M1 and M2 segments) within 8 hours of symptom onset. Patients who are ineligible for intravenous tissue plasminogen activator (IV t-PA) or who fail IV t-PA therapy are candidates for treatment.

Penumbra Aspiration Tubing

As part of the Penumbra System, the Penumbra Sterile Aspiration Tubing is indicated to connect the Penumbra Reperfusion Catheters to the Penumbra Aspiration Pump.

Penumbra Aspiration Pump

The Penumbra Aspiration Pump is indicated as a vacuum source for Penumbra Aspiration Systems.

Indications for use as stated in the FDA summary.

Also cleared against K190010

1 other device cites the same predicate.

  • K191946Penumbra System Penumbra JET 7XPenumbra, Inc. · 20204 Class I recalls

More from Penumbra, Inc.

88 FDA decisions under this applicant name. See the company

  • K262904INDIGO® Aspiration SystemPenumbra, Inc. · 2026
  • K250690Penumbra System (Thunderbolt Aspiration Tubing)Penumbra, Inc. · 20261 recall
  • K260599INDIGO® Aspiration System – INDIGO LinkPenumbra, Inc. · 2026
  • K251949INDIGO® Aspiration System - Lightning Flash Aspiration Tubing with LINKPenumbra, Inc. · 2026
  • K252612INDIGO® Aspiration System – Lightning Flash Aspiration Tubing; INDIGO® Aspiration System – Lightning Bolt…Penumbra, Inc. · 2025

Recent decisions in NRY

The NRY category page

  • K262021Toro 71 Aspiration Catheter; Toro Aspiration TubingToro Neurovascular, Inc. · 2026
  • K263266Route 92 Medical Full Length 046 Reperfusion System and Aspiration Tubing SetRoute 92 Medical, Inc. · 2026
  • K261089Radical 064 Reperfusion Catheter; Radical 076 Reperfusion Catheter; Radical Aspiration Tubing KitMaduro Medical, Inc. · 2026
  • K260617Tigertriever 13 Ultra Revascularization DeviceRapid Medical Ltd. · 2026
  • K262398CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing setCERENOVUS, Inc. · 2026

https://510kreport.com/device/K202251 · printed Nov 6, 2026

Cite this page

510(k) Report. “K202251: Penumbra System (Penumbra JET 7 Reperfusion Catheter with Xtra Flex Technology; Penumbra JET 7MAX).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K202251

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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