510(k) Report

510(k) · Cleared

Cleared

Aristotle 14 Guidewire; Aristotle 18 Guidewire; Aristotle 24 Guidewire; Zoom Wire 14 Guidewire

K253579510(k) TraditionalCleared Apr 29, 2026163-day reviewClass II21 CFR 870.1330

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

Scientia Vascular, Inc. · MOF Guide, Wire, Catheter, Neurovasculature

Cleared on Apr 29, 2026 as substantially equivalent to K173235 (Scientia Vascular, LLC, 2018) and 2 other predicates after a 163-day review. Its family tree reaches back 6 generations to 2000.

Decided
Apr 29, 2026
Review
163 days
Class
Class II
Product code
MOF
Recalls
None
Predicates
3

Its longest line of descent runs back 6 generations to K002212 (2000). 7 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 6 generations backK002212 Mirage Hydrophilic Guidewire, Model 103-0608Micro Therapeutics, Inc. · 2000
  2. 5 generations backK032146 PVS 1300 Synchro 0.014 & PVS 1600 Synchro 0.010 Guide WiresPrecision Vascular Systems, Inc. · 2003 · Recalled
  3. 4 generations backK173235 Aristotle 14 Guidewire, 200cm, Soft Profile, Aristotle 14 Guidewire…Scientia Vascular, LLC · 2018
  4. 3 generations backK183608 Aristotle 18 Guidewire, 200cm, Soft Profile ; Aristotle 18…Scientia Vascular, LLC · 2019
  5. 2 generations backK192783 Aristotle 24 Guidewire, 200cm, Soft Profile ; Aristotle 24…Scientia Vascular, LLC · 2019
  6. 1 generation backK231954 Aristotle 18 Guidewire; Aristotle 24 GuidewireScientia Vascular, Inc. · 2023
  7. This deviceK253579 Aristotle 14 Guidewire; Aristotle 18 Guidewire; Aristotle 24…Scientia Vascular, Inc. · 2026
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K002212Mirage Hydrophilic Guidewire, Model 103-0608Micro Therapeutics, Inc.2000—
−5K032146PVS 1300 Synchro 0.014 & PVS 1600 Synchro 0.010 Guide WiresPrecision Vascular Systems, Inc.20031
−4K173235Aristotle 14 Guidewire, 200cm, Soft Profile, Aristotle 14 Guidewire, 200cm…Scientia Vascular, LLC2018—
−3K183608Aristotle 18 Guidewire, 200cm, Soft Profile ; Aristotle 18 Guidewire, 200cm…Scientia Vascular, LLC2019—
−2K192783Aristotle 24 Guidewire, 200cm, Soft Profile ; Aristotle 24 Guidewire, 200cm…Scientia Vascular, LLC2019—
−1K231954Aristotle 18 Guidewire; Aristotle 24 GuidewireScientia Vascular, Inc.2023—
0 (this device)K253579Aristotle 14 Guidewire; Aristotle 18 Guidewire; Aristotle 24 Guidewire; Zoom…Scientia Vascular, Inc.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
202010
FIG. 1 — Lineage of K253579, 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 MOF? 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 MOF device

  1. #1 K253168 0.014” Willow Guidewirescore 17.9 · 6 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
*K173235Aristotle 14 Guidewire, 200cm, Soft Profile, Aristotle 14 Guidewire, 200cm, Support…
Summary page 6
…uide Wire per 21 CFR 870.1330 Primary Product Code: MOF Subsequent Product Code DQX Predicate Device: Aristotle 14 Guidewire (K173235) Aristotle 18 Guidewire Trade Name: Aristotle 18 Guidewire Common Name: Guidew…
Scientia Vascular, LLC2018—
*K231954Aristotle 18 Guidewire; Aristotle 24 Guidewire
Summary page 6
…uide Wire per 21 CFR 870.1330 Primary Product Code: MOF Subsequent Product Code DQX Predicate Device: Aristotle 18 Guidewire (K231954) Aristotle 24 Guidewire Trade Name: Aristotle 24 Guidewire Common Name: Guidew…
Scientia Vascular, Inc.2023—
*K201760Zoom 14 Guidewire
Summary page 6
…ter Guide Wire per 21 CFR 870.1330 Primary Product Code: MOF Subsequent Product Code DQX Predicate Device: Zoom 14 Guidewire (K201760) 2 Scientia Vascular, Inc. K253…
Scientia Vascular, LLC2020—

Also cleared against K173235: 5 other devices →

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 26 years and passes through 4 companies; a new generation was cleared every 3.0 years on median.
  • 1 of the 7 ancestors has a recall of any class.
  • 5 other devices also cite its predicate K173235.

How does its category compare?

All MOF devices

MOF Guide, Wire, Catheter, Neurovasculature: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, this device’s year, is highlighted.

FDA decisions per year · MOF

11so far in 2026, the most since 2007

2011: 22014: 22015: 32016: 42017: 12018: 22019: 42020: 42022: 12023: 42024: 22025: 52026 (partial year): 11
2007high 11 (2026) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MOF

172in 2025

2015: 133 days median2016: 61 days median2019: 58 days median2020: 36 days median2023: 199 days median2025: 172 days median2026 (partial year): 192 days median
2007high 199 (2023) · low 36 (2020)2026

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

Recalls per year · MOF

No recall names MOF since 2007.

Adverse event reports per year · MOF

135in 2025

2008: 12012: 22013: 22015: 52016: 32017: 152018: 112019: 122020: 182021: 392022: 922023: 912024: 952025: 135
2007high 135 (2025) · low 0 (2007)2025

MAUDE reports naming product code MOF, 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
20080—01
20090—00
20100—00
20112—00
20120—02
20130—02
20142—00
2015313305
201646103
20171—015
20182—011
2019458012
2020436018
20210—039
20221—092
20234199091
20242—095
202551720135
2026111920—

What is it indicated for?

Aristotle 14 Guidewire The Aristotle 14 Guidewire is intended for general vascular use within the neuro and peripheral vasculatures to introduce and position catheters and other interventional devices. The guidewire is not intended for use in the coronary vasculature. Aristotle 18 Guidewire The Aristotle 18 Guidewire is intended for general vascular use within the neuro and peripheral vasculatures to introduce and position catheters and other…

Read the full statement (158 words)

Aristotle 14 Guidewire

The Aristotle 14 Guidewire is intended for general vascular use within the neuro and peripheral vasculatures to introduce and position catheters and other interventional devices. The guidewire is not intended for use in the coronary vasculature.

Aristotle 18 Guidewire

The Aristotle 18 Guidewire is intended for general vascular use within the neuro and peripheral vasculatures to introduce and position catheters and other interventional devices. The guidewire is not intended for use in the coronary vasculature.

Aristotle 24 Guidewire

The Aristotle 24 Guidewire is intended for general vascular use within the neuro and peripheral vasculatures to introduce and position catheters and other interventional devices. The guidewire is not intended for use in the coronary vasculature.

Zoom Wire 14 Guidewire

The Zoom Wire 14 Guidewire is intended for general vascular use within the neuro and peripheral vasculatures to introduce and position catheters and other interventional devices. The guidewire is not intended for use in the coronary vasculature.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K253579: Aristotle 14 Guidewire; Aristotle 18 Guidewire; Aristotle 24 Guidewire; Zoom Wire 14 Guidewire.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K253579

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Record history
  • FDA decision record loaded Oct 30, 2026
  • Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026