510(k) Report

510(k) · Cleared

Cleared

Nanocross Elite .14 Over-the-Wire Pta, Balloon Dilation Catheter

K132777510(k) TraditionalCleared Sep 26, 201321-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

Ev3, Inc. · LIT Catheter, Angioplasty, Peripheral, Transluminal

Cleared on Sep 26, 2013 as substantially equivalent to K082854 (Ev3, Inc., 2008) and 2 other predicates after a 21-day review. Its family tree reaches back 9 generations to 2000. 6 later devices descend from it.

Decided
Sep 26, 2013
Review
21 days
Class
Class II
Product code
LIT
Recalls
None
Predicates
3

Its longest line of descent runs back 9 generations to K001134 (2000). 21 ancestors in all. 6 later devices descend from it, 1 citing it directly.

  1. Root · 9 generations backK001134 Gazelle Balloon Dilatation CatheterBoston Scientific Corp · 2000
  2. 5 generations between
  3. 3 generations backK093286 Powercross .018 Otw Pta Dilation CatheterEv3, Inc. · 2009 · Recalled
  4. 2 generations backK123544 Rapidcross Pta Rapid Exchange, Balloon Dilatation CatheterEv3, Inc. · 2013
  5. 1 generation backK130911 Rapidcross Pta Rapid Exchange Balloon Dilatation CatheterEv3, Inc. · 2013
  6. This deviceK132777 Nanocross Elite .14 Over-the-Wire Pta, Balloon Dilation CatheterEv3, Inc. · 2013
  7. Descendant · cites it directly · 5 of its ownK141118 Nanocross Eite 0.014 Over-the-Wire Pta Balloon Dilatation CatheterEv3, Inc. · 2014 · Recalled
  8. Descendant · 2 generations on · 1 of its ownK160256 Polux , Minerva and Atropos PTA Balloon Dilatation CatheterBrosmed Medical Co., Ltd. · 2016
  9. Descendant · 2 generations on · 1 of its ownK142459 Ebony PTA 0.014 RX Peripheral Dilatation CatheterNatec Medical, Ltd. · 2015
  10. Descendant · 3 generations on · 0 of its ownK243704 Parafleet SC 014 PTA Balloon Dilatation Catheter; Parafleet SC 018…Brosmed Medical Co., Ltd. · 2025
  11. Descendant · 2 generations on · 0 of its ownK160941 Castor, Achilles and Hermes NC PTA Balloon Dilatation CatheterBrosmed Medical Co., Ltd. · 2016 · Recalled
Show all 9 generations
  1. Root · 9 generations backK001134 Gazelle Balloon Dilatation CatheterBoston Scientific Corp · 2000
  2. 8 generations backK021735 Boston Scientific Ultra-Soft SV Balloon Dilatation CatheterBoston Scientific Scimed, Inc. · 2002 · Recalled
  3. 7 generations backK050389 Ultra-Soft SV Balloon Dilatation CatheterBoston Scientific Corp · 2005
  4. 6 generations backK053116 Sterling Otw Pta Balloon Dilatation Catheter, Model H74939032-XxxxxxBoston Scientific Corp · 2005
  5. 5 generations backK072283 Dorado Pta Balloon Dilatation CatheterBard Peripheral Vascular, Inc. · 2007 · Recalled
  6. 4 generations backK082579 Evercross .035 Otw Pta Dilatation CatheterEv3, Inc. · 2008 · Recalled
  7. 3 generations backK093286 Powercross .018 Otw Pta Dilation CatheterEv3, Inc. · 2009 · Recalled
  8. 2 generations backK123544 Rapidcross Pta Rapid Exchange, Balloon Dilatation CatheterEv3, Inc. · 2013
  9. 1 generation backK130911 Rapidcross Pta Rapid Exchange Balloon Dilatation CatheterEv3, Inc. · 2013
  10. This deviceK132777 Nanocross Elite .14 Over-the-Wire Pta, Balloon Dilation CatheterEv3, Inc. · 2013

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

2014: 12015: 22016: 22025: 1
2014high 2 (2015) · low 0 (2017)2026

Most influential descendants

Showing 5 of 6 · See all
  • K141118Nanocross Eite 0.014 Over-the-Wire Pta Balloon Dilatation CatheterEv3, Inc. · 2014 · cites it directly5descendants
  • K160256Polux , Minerva and Atropos PTA Balloon Dilatation CatheterBrosmed Medical Co., Ltd. · 2016 · 2 generations on1descendant
  • K142459Ebony PTA 0.014 RX Peripheral Dilatation CatheterNatec Medical, Ltd. · 2015 · 2 generations on1descendant
  • K243704Parafleet SC 014 PTA Balloon Dilatation Catheter; Parafleet SC 018 PTA Balloon…Brosmed Medical Co., Ltd. · 2025 · 3 generations on0descendants
  • K160941Castor, Achilles and Hermes NC PTA Balloon Dilatation CatheterBrosmed Medical Co., Ltd. · 2016 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K001134Gazelle Balloon Dilatation CatheterBoston Scientific Corp2000—
−8K021735Boston Scientific Ultra-Soft SV Balloon Dilatation CatheterBoston Scientific Scimed, Inc.200223
−7K050389Ultra-Soft SV Balloon Dilatation CatheterBoston Scientific Corp2005—
−6K053116Sterling Otw Pta Balloon Dilatation Catheter, Model H74939032-XxxxxxBoston Scientific Corp2005—
−5K072283Dorado Pta Balloon Dilatation CatheterBard Peripheral Vascular, Inc.200715
−4K082579Evercross .035 Otw Pta Dilatation CatheterEv3, Inc.20081
−3K093286Powercross .018 Otw Pta Dilation CatheterEv3, Inc.20092
−2K123544Rapidcross Pta Rapid Exchange, Balloon Dilatation CatheterEv3, Inc.2013—
−1K130911Rapidcross Pta Rapid Exchange Balloon Dilatation CatheterEv3, Inc.2013—
0 (this device)K132777Nanocross Elite .14 Over-the-Wire Pta, Balloon Dilation CatheterEv3, Inc.2013—
+1K141118Nanocross Eite 0.014 Over-the-Wire Pta Balloon Dilatation CatheterEv3, Inc.20141
+2K160256Polux , Minerva and Atropos PTA Balloon Dilatation CatheterBrosmed Medical Co., Ltd.2016—
+2K142459Ebony PTA 0.014 RX Peripheral Dilatation CatheterNatec Medical, Ltd.2015—
+3K243704Parafleet SC 014 PTA Balloon Dilatation Catheter; Parafleet SC 018 PTA Balloon…Brosmed Medical Co., Ltd.2025—
+2K160941Castor, Achilles and Hermes NC PTA Balloon Dilatation CatheterBrosmed Medical Co., Ltd.20161

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200110
200210
200420
200520
200620
200820
200920

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201410
201520
201620
202510
FIG. 1 — Lineage of K132777, 2000–2025Source: 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 LIT? 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 LIT device

  1. #1 K241040 Amethyst HP PTA OTW 0.035 Catheterscore 13.9 · 9 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) 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.

TypeNumberDeviceApplicantDecidedRecalls
*K082854Nanocorss .014 Otw Pta Dilatation Catheter
Summary page 1
…duct Code LIT) Classification Panel Cardiovascular Predicate Devices NanoCrossm .01 V4OTW PTA Dilatation Catheter (K082854, K090849), RapidCross Tm PTA Rapid Exchange Balloon…
Ev3, Inc.20081
*K090849Modification to: Nanocross 0.14 Otw Pta Dilatation Catheter, Models AB14W020210090…
Summary page 1
…Cardiovascular Predicate Devices NanoCrossm .01 V4OTW PTA Dilatation Catheter (K082854, K090849), RapidCross Tm PTA Rapid Exchange Balloon Dilatation Catheter (K1 30911I).…
Ev3, Inc.20091
*K130911Rapidcross Pta Rapid Exchange Balloon Dilatation Catheter
Summary page 1
…54, K090849), RapidCross Tm PTA Rapid Exchange Balloon Dilatation Catheter (K1 30911I). Intended use The NanoCross" Elite 0.0 14" Over-the-Wire PTA Balloon…
Ev3, Inc.2013—

Also cleared against K082854: 2 other devices →

What descends from it? (6)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K141118Nanocross Eite 0.014 Over-the-Wire Pta Balloon Dilatation CatheterEv3, Inc.20145

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 13 years and passes through 4 companies; a new generation was cleared every 1.2 years on median.
  • 6 of the 21 ancestors have a recall of any class.
  • Of its descendants, K141118 (Ev3, Inc., 2014) has gone furthest, with 5 descendants of its own.
  • 2 other devices also cite its predicate K082854.

How does its category compare?

All LIT devices

LIT Catheter, Angioplasty, Peripheral, Transluminal: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.

FDA decisions per year · LIT

3in 2025

2007: 62008: 82009: 72010: 132011: 102012: 192013: 142014: 122015: 192016: 112017: 92018: 62019: 42020: 92021: 42022: 82023: 62024: 62025: 32026 (partial year): 4
2007high 19 (2012) · low 3 (2025)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LIT

90in 2025

2007: 64 days median2008: 53 days median2009: 29 days median2010: 78 days median2011: 82 days median2012: 29 days median2013: 79 days median2014: 90 days median2015: 112 days median2016: 116 days median2017: 57 days median2018: 118 days median2019: 40 days median2020: 125 days median2021: 61 days median2022: 122 days median2023: 167 days median2024: 43 days median2025: 90 days median2026 (partial year): 205 days median
2007high 205 (2026) · low 29 (2009)2026

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

Recalls per year · LIT

1in 2025

2009: 22010: 12013: 2, 2 Class I2014: 32016: 12018: 22019: 32021: 12024: 22025: 1
2007high 3 (2014) · low 0 (2007)2026

Class I (2 since 2007) Class II/III not classified

Adverse event reports per year · LIT

2,073in 2025

2007: 5772008: 5132009: 6232010: 8092011: 8572012: 1,2772013: 1,2422014: 1,1782015: 1,2792016: 1,5292017: 2,0812018: 2,1882019: 2,4052020: 2,4432021: 2,4922022: 2,1552023: 1,8072024: 1,9132025: 2,073
2007high 2,492 (2021) · low 513 (2008)2025

MAUDE reports naming product code LIT, 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
20076640577
20088530513
20097292623
201013781809
201110820857
2012192901,277
201314792 (2)1,242
2014129031,178
20151911201,279
20161111611,529
201795702,081
2018611822,188
201944032,405
2020912502,443
202146112,492
2022812202,155
2023616701,807
202464321,913
202539012,073
202642050—

What is it indicated for?

The NanoCrossTM Elite 0.014" Over-the-Wire PTA Balloon 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 arteriovenous dialysis fistulae. This device is also indicated for stent post-dilatation in the peripheral vasculature.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K132777: Nanocross Elite .14 Over-the-Wire Pta, Balloon Dilation Catheter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K132777

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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