510(k) Report

510(k) · Cleared

Cleared

Vascutrak Pta Dilatation Catheter

K103459510(k) TraditionalCleared Dec 13, 201019-day reviewClass II21 CFR 870.1250

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

C.R. Bard, Inc. · PNO Catheter, Percutaneous, Cutting/Scoring

Cleared on Dec 13, 2010 as substantially equivalent to K082343 (Ymed, Inc., 2008) and 2 other predicates after a 19-day review. Its family tree reaches back 6 generations to 2000. 36 later devices descend from it.

Decided
Dec 13, 2010
Review
19 days
Class
Class II
Product code
PNO
Recalls
None
Predicates
3

Its longest line of descent runs back 6 generations to K001134 (2000). 25 ancestors in all, the oldest K971010 (1997). 36 later devices descend from it, 6 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2008: 1 other ancestor2007: 1 other ancestor2006: 2 other ancestors2005: 4 other ancestors2002: 3 other ancestors2001: 1 other ancestor2003: 3 other ancestors2004: 1 other ancestor2000: 2 other ancestors1997: 1 other ancestor2019: 2 descendants cleared2011: 1 descendant cleared2017: 3 descendants cleared2014: 1 descendant cleared2025: 3 descendants cleared2016: 2 descendants cleared2013: 1 descendant cleared2015: 2 descendants cleared2026: 4 descendants cleared2020: 3 descendants cleared2024: 6 descendants cleared2018: 2 descendants cleared2021: 2 descendants cleared2022: 4 descendants clearedK001134 · Gazelle Balloon Dilatation Catheter · Boston Scientific Corp · 2000K021735 · Boston Scientific Ultra-Soft SV Balloon Dilatation Catheter · Boston Scientific Scimed, Inc. · 2002 · recalledK050389 · Ultra-Soft SV Balloon Dilatation Catheter · Boston Scientific Corp · 2005K053116 · Sterling Otw Pta Balloon Dilatation Catheter, Model H74939032-Xxxxxx · Boston Scientific Corp · 2005K072283 · Dorado Pta Balloon Dilatation Catheter · Bard Peripheral Vascular, Inc. · 2007 · recalledK083657 · Conquest Pta Balloon Dilatation Catheter · C.R. Bard, Inc. · 2008 · recalled1995200020052010201520202025
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 5 other ancestors3 generations back: 4 other ancestors4 generations back: 7 other ancestors5 generations back: 2 other ancestors 1 generation forward: 6 descendants2 generations forward: 7 descendants3 generations forward: 9 descendants4 generations forward: 7 descendants5 generations forward: 6 descendants6 generations forward: 1 descendant K083657 · Conquest Pta Balloon Dilatation Catheter · C.R. Bard, Inc. · 2008 · recalledK072283 · Dorado Pta Balloon Dilatation Catheter · Bard Peripheral Vascular, Inc. · 2007 · recalledK053116 · Sterling Otw Pta Balloon Dilatation Catheter, Model H74939032-Xxxxxx · Boston Scientific Corp · 2005K050389 · Ultra-Soft SV Balloon Dilatation Catheter · Boston Scientific Corp · 2005K021735 · Boston Scientific Ultra-Soft SV Balloon Dilatation Catheter · Boston Scientific Scimed, Inc. · 2002 · recalledK001134 · Gazelle Balloon Dilatation Catheter · Boston Scientific Corp · 2000−50+5
  1. Root · 6 generations backK001134 Gazelle Balloon Dilatation CatheterBoston Scientific Corp · 2000
  2. 5 generations backK021735 Boston Scientific Ultra-Soft SV Balloon Dilatation CatheterBoston Scientific Scimed, Inc. · 2002 · Recalled
  3. 4 generations backK050389 Ultra-Soft SV Balloon Dilatation CatheterBoston Scientific Corp · 2005
  4. 3 generations backK053116 Sterling Otw Pta Balloon Dilatation Catheter, Model H74939032-XxxxxxBoston Scientific Corp · 2005
  5. 2 generations backK072283 Dorado Pta Balloon Dilatation CatheterBard Peripheral Vascular, Inc. · 2007 · Recalled
  6. 1 generation backK083657 Conquest Pta Balloon Dilatation CatheterC.R. Bard, Inc. · 2008 · Recalled
  7. This deviceK103459 Vascutrak Pta Dilatation CatheterC.R. Bard, Inc. · 2010
  8. Descendant · cites it directly · 29 of its ownK112182 Angiosculpt Pta Scoring Balloon CatheterAngioscore, Inc. · 2011
  9. Descendant · 2 generations on · 28 of its ownK122685 Angiosculpt Pta Scoring Balloon CatheterAngioscore, Inc. · 2013
  10. Descendant · cites it directly · 24 of its ownK133998 Angiosculpt Pta Scoring Balloon with Hydrocross CaotingAngioscore, Inc. · 2014
  11. Descendant · 2 generations on · 16 of its ownK142983 AngioSculpt PTA Scoring Balloon Catheter with HydroCross CoatingAngioscore, Inc. · 2015
  12. Descendant · cites it directly · 13 of its ownK161384 Lithoplasty Peripheral Balloon Dilatation Catheter, Lithoplasty…Shockwave Medical, Inc. · 2016

Showing 5 of 36 descendants. See all descendants

Descendants cleared per year

2011: 12013: 12014: 12015: 22016: 22017: 32018: 22019: 22020: 32021: 22022: 42024: 62025: 32026: 4
2011high 6 (2024) · low 0 (2012)2026

Most influential descendants

Showing 5 of 36 · See all
  • K112182Angiosculpt Pta Scoring Balloon CatheterAngioscore, Inc. · 2011 · cites it directly29descendants
  • K122685Angiosculpt Pta Scoring Balloon CatheterAngioscore, Inc. · 2013 · 2 generations on28descendants
  • K133998Angiosculpt Pta Scoring Balloon with Hydrocross CaotingAngioscore, Inc. · 2014 · cites it directly24descendants
  • K142983AngioSculpt PTA Scoring Balloon Catheter with HydroCross CoatingAngioscore, Inc. · 2015 · 2 generations on16descendants
  • K161384Lithoplasty Peripheral Balloon Dilatation Catheter, Lithoplasty Generator and Connector…Shockwave Medical, Inc. · 2016 · cites it directly13descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K001134Gazelle Balloon Dilatation CatheterBoston Scientific Corp2000—
−5K021735Boston Scientific Ultra-Soft SV Balloon Dilatation CatheterBoston Scientific Scimed, Inc.200223
−4K050389Ultra-Soft SV Balloon Dilatation CatheterBoston Scientific Corp2005—
−3K053116Sterling Otw Pta Balloon Dilatation Catheter, Model H74939032-XxxxxxBoston Scientific Corp2005—
−2K072283Dorado Pta Balloon Dilatation CatheterBard Peripheral Vascular, Inc.200715
−1K083657Conquest Pta Balloon Dilatation CatheterC.R. Bard, Inc.20082
0 (this device)K103459Vascutrak Pta Dilatation CatheterC.R. Bard, Inc.2010—
+1K112182Angiosculpt Pta Scoring Balloon CatheterAngioscore, Inc.2011—
+2K122685Angiosculpt Pta Scoring Balloon CatheterAngioscore, Inc.2013—
+1K133998Angiosculpt Pta Scoring Balloon with Hydrocross CaotingAngioscore, Inc.2014—
+2K142983AngioSculpt PTA Scoring Balloon Catheter with HydroCross CoatingAngioscore, Inc.2015—
+1K161384Lithoplasty Peripheral Balloon Dilatation Catheter, Lithoplasty Generator and…Shockwave Medical, Inc.2016—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199710
200020
200110
200230
200330
200410
200540
200620
200710
200810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201110
201310
201410
201520
201620
201730
201820
201920
202030
202120
202240
202460
202530
202640
FIG. 1 — Lineage of K103459, 2000–2026Source: 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 PNO? 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 PNO device

  1. #1 K261778 JADE SCORE PTA Scoring Balloon Dilatation…score 14.1 · 8 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? (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.

TypeNumberDeviceApplicantDecidedRecalls
*K082343Vascutrak 2, Models: V14 and V18
Summary page 4
…s Catheter (21 CFR 870.1250, Product Code DQY) Classification: Class |l Classification Panel: Cardiovascular Predicate Devices: » Vascutrak™ 2 PTA Dilatation Catheter (K082343; cleared September 11, 2008) » Conquest™ PTA Balloon Dilatation Catheter (K083657; cleared December 24, 2008) * Dorado™ PTA Bal…
Ymed, Inc.2008—
*K083657Conquest Pta Balloon Dilatation Catheter
Summary page 4
…ion Panel: Cardiovascular Predicate Devices: » Vascutrak™ 2 PTA Dilatation Catheter (K082343; cleared September 11, 2008) » Conquest™ PTA Balloon Dilatation Catheter (K083657; cleared December 24, 2008) * Dorado™ PTA Balloon Dilatation Catheter (K072283; cleared September 19, 2007) Bard Peripheral Vas…
C.R. Bard, Inc.20082
*K072283Dorado Pta Balloon Dilatation Catheter
Summary page 4
…heter (K082343; cleared September 11, 2008) » Conquest™ PTA Balloon Dilatation Catheter (K083657; cleared December 24, 2008) * Dorado™ PTA Balloon Dilatation Catheter (K072283; cleared September 19, 2007) Bard Peripheral Vascular, Inc. [BZNBID Traditional 510(k) Vascutrak PTA Dilatation…
Bard Peripheral Vascular, Inc.200715

Also cleared against K082343: 6 other devices →

What descends from it? (36)

See all 36

6 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K112182Angiosculpt Pta Scoring Balloon CatheterAngioscore, Inc.201129
K133998Angiosculpt Pta Scoring Balloon with Hydrocross CaotingAngioscore, Inc.201424
K161384Lithoplasty Peripheral Balloon Dilatation Catheter, Lithoplasty Generator and Connector…Shockwave Medical, Inc.201613
K163420UltraScore Focused Force PTA BalloonBard Peripheral Vascular, Inc.20173
K242254D·Kutting™ LL Peripheral Scoring Balloon Dilatation CatheterDk Medical Technology Co., Ltd.20250
K182713Scoreflex PTA Scoring Balloon CatheterOrbusneich Medical Trading, Inc.20190

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 10 years and passes through 4 companies; a new generation was cleared every 1.9 years on median.
  • 5 of the 25 ancestors have a recall of any class.
  • Of its descendants, K112182 (Angioscore, Inc., 2011) has gone furthest, with 29 descendants of its own.
  • 6 other devices also cite its predicate K082343.

How does its category compare?

All PNO devices

PNO Catheter, Percutaneous, Cutting/Scoring: FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, this device’s year, is highlighted.

FDA decisions per year · PNO

2in 2025

2007: 32008: 42009: 12010: 32011: 22012: 12013: 12014: 12015: 42016: 12017: 32019: 12020: 42021: 12022: 22024: 42025: 22026 (partial year): 3
2007high 4 (2008) · low 0 (2018)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PNO

246in 2024

2007: 61 days median2008: 28 days median2010: 23 days median2015: 84 days median2017: 74 days median2020: 94 days median2024: 246 days median2026 (partial year): 110 days median
2007high 246 (2024) · low 23 (2010)2026

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

Recalls per year · PNO

No recall names PNO since 2007.

Adverse event reports per year · PNO

511in 2025

2016: 92017: 262018: 552019: 812020: 1212021: 902022: 752023: 3042024: 5372025: 511
2007high 537 (2024) · low 0 (2007)2025

MAUDE reports naming product code PNO, 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
200736100
200842800
20091—00
201032300
20112—00
20121—00
20131—00
20141—00
201548400
20161—09
2017374026
20180—055
20191—081
20204940121
20211—090
20222—075
20230—0304
202442460537
20252—0511
202631100—

What is it indicated for?

The Vascutrak™ PTA Dilatation Catheter is intended to dilate stenoses in the iliac, femoral, ilio-femoral, popliteal, infra-popliteal and renal arteries and for the treatment of obstructive lesions of native or synthetic arterioveneous dialysis fistulae. This device is also recommended for post-dilatation of balloon expandable stents, self-expanding stents, and stent grafts in the peripheral 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. “K103459: Vascutrak Pta Dilatation Catheter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K103459

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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