510(k) Report

510(k) · Cleared

Cleared

MindsEye Expandable Port

K202072510(k) TraditionalCleared Aug 26, 202030-day reviewClass II21 CFR 882.4800

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

Minnetronix Neuro, Inc. · GZT Retractor, Self-Retaining, For Neurosurgery

Cleared on Aug 26, 2020 as substantially equivalent to K172433 (Nico Corporation, 2017) after a 30-day review. Its family tree reaches back 6 generations to 2000. 1 of the 11 devices in its family, counting itself, has a Class I recall.

Decided
Aug 26, 2020
Review
30 days
Class
Class II
Product code
GZT
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K002931 (2000). 10 ancestors in all, the oldest K830332 (1983). No later device cites it as a predicate yet. 1 of the 11 devices in this family, counting this one, has a Class I recall.

  1. Root · 6 generations backK002931 Metrx SystemMedtronic Sofamor Danek, Inc. · 2000
  2. 5 generations backK043602 Quadrant Retractor SystemMedtronic Sofamor Danek · 2005
  3. 4 generations backK060973 Vycor Surgical Access SystemsVycor Medical, LLC · 2006 · Recalled (Class I)
  4. 3 generations backK120691 Brain PortNico Corporation · 2012 · Recalled
  5. 2 generations backK150378 NICO BrainPath & Accessories, NICO BrainPath, NICO Shepherd's HookNico Corporation · 2015
  6. 1 generation backK172433 NICO BrainPathNico Corporation · 2017
  7. This deviceK202072 MindsEye Expandable PortMinnetronix Neuro, Inc. · 2020

Class I recalls in this family

View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K002931Metrx SystemMedtronic Sofamor Danek, Inc.2000—
−5K043602Quadrant Retractor SystemMedtronic Sofamor Danek2005—
−4K060973Vycor Surgical Access SystemsVycor Medical, LLC2006Class I
−3K120691Brain PortNico Corporation20122
−2K150378NICO BrainPath & Accessories, NICO BrainPath, NICO Shepherd's HookNico Corporation2015—
−1K172433NICO BrainPathNico Corporation2017—
0 (this device)K202072MindsEye Expandable PortMinnetronix Neuro, Inc.2020—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198310
198920
200410
FIG. 1 — Lineage of K202072, 2000–2020Source: 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.

1 device in this family has 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 GZT device

  1. #1 K252995 Durashield Device Kitscore 12.6 · 3 generations · no Class I recall
  2. #2 Held for the reportin the report
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What was it cleared against? (1)

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
*K172433NICO BrainPath
Summary page 4
…Neurological Devices Panel 5.3 IDENTIFICATION OF PREDICATE DEVICE The predicate device for the MindsEye Expandable Port is the Nico® BrainPath® (K172433) with reference to the Vycor VBAS (K060973). 5.4 DEVICE DESCRIPTION The MindsEye Expandable Port is a…
Nico Corporation2017—
†K060973Vycor Surgical Access SystemsVycor Medical, LLC2006Class I

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (1 Class I)

No FDA recall names this device.

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.

  • K060973Vycor Surgical Access SystemsVycor Medical, LLC · 2006 · 4 generations back · ◆ on the line of descent in FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 20 years and passes through 5 companies; a new generation was cleared every 3.0 years on median.
  • 3 of the 10 ancestors have a recall of any class; 1 has a Class I recall.

How does its category compare?

All GZT devices

GZT Retractor, Self-Retaining, For Neurosurgery: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · GZT

1in 2022

2007: 22009: 12010: 12011: 12012: 22015: 12016: 12017: 32018: 12020: 12021: 12022: 12026 (partial year): 1
2007high 3 (2017) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GZT

280in 2017

2017: 280 days median
2007high 280 (2017)2026

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

Recalls per year · GZT

1in 2012

2007: 12012: 1, 1 Class I
2007high 1 (2007) · low 0 (2008)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · GZT

1in 2025

2009: 12010: 42011: 42012: 62013: 122014: 162015: 42016: 52017: 92018: 32019: 52020: 32021: 22022: 42023: 22024: 82025: 1
2007high 16 (2014) · low 0 (2007)2025

MAUDE reports naming product code GZT, 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
20072—10
20080—00
20091—01
20101—04
20111—04
20122—1 (1)6
20130—012
20140—016
20151—04
20161—05
2017328009
20181—03
20190—05
20201—03
20211—02
20221—04
20230—02
20240—08
20250—01
20261—0—

What is it indicated for?

The Expandable Port is intended to provide access, allow visualization of the surgical field, and retraction of soft tissue during neurological cranial surgery.

The device is indicated for use in surgery during which subcortical access is required.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K202072: MindsEye Expandable Port.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K202072

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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