510(k) Report

510(k) · Cleared

Cleared

Sugita Avm Microclip

K960037510(k) TraditionalCleared Feb 5, 1997399-day reviewClass II21 CFR 882.5200

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

Mizuho America, Inc. · HCH Clip, Aneurysm

Cleared on Feb 5, 1997 as substantially equivalent to K902544 (Codman & Shurtleff, Inc., 1990) after a 399-day review. Its family tree reaches back 1 generation to 1990. 1 later device descends from it.

Decided
Feb 5, 1997
Review
399 days
Class
Class II
Product code
HCH
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K902544 (1990). 1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2022: 1 descendant clearedK902544 · Sundt Avm Micro Clip · Codman & Shurtleff, Inc. · 19901990200020102020
Descendants, by generation 1 generation forward: 1 descendant K902544 · Sundt Avm Micro Clip · Codman & Shurtleff, Inc. · 19900
  1. Root · 1 generation backK902544 Sundt Avm Micro ClipCodman & Shurtleff, Inc. · 1990
  2. This deviceK960037 Sugita Avm MicroclipMizuho America, Inc. · 1997
  3. Descendant · cites it directly · 0 of its ownK211183 Sugita AVM MicroclipsMizuho America, Inc. · 2022

Most influential descendants

Showing 1 of 1 · See all
  • K211183Sugita AVM MicroclipsMizuho America, Inc. · 2022 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K902544Sundt Avm Micro ClipCodman & Shurtleff, Inc.1990—
0 (this device)K960037Sugita Avm MicroclipMizuho America, Inc.1997—
+1K211183Sugita AVM MicroclipsMizuho America, Inc.2022—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202210
FIG. 1 — Lineage of K960037, 1990–2022Source: 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 HCH? 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 HCH device

  1. #1 K211183 Sugita AVM Microclipsscore 3.2 · 2 generations · no Class I recall
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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
*K902544Sundt Avm Micro Clip
Summary page 1
…roclip Common Name: AVM Clip Classification Name: Could not be determined Legally Marketed Devices to Which Substantial Equivalence is claimed: Sundt AVM Micro Clip - K902544 SUGITA The leading name in neurosurgical instrumentation 510(k) SUMMARY-continued Sugita AVM Microclip Descript…
Codman & Shurtleff, Inc.1990—

Also cleared against K902544: 1 other device →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K211183Sugita AVM MicroclipsMizuho America, Inc.20220

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?

  • Its one ancestor has no recall.
  • Of its descendants, K211183 (Mizuho America, Inc., 2022) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K902544.

How does its category compare?

All HCH devices

HCH Clip, Aneurysm: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · HCH

1in 2022

2007: 12008: 12009: 22014: 12019: 12022: 1
2007high 2 (2009) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HCH

Too few HCH 510(k)s in any year since 2007 to give a median.

Recalls per year · HCH

2in 2013

2013: 2
2007high 2 (2013) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · HCH

2in 2025

2010: 42012: 42013: 32014: 132015: 92016: 52017: 12018: 192019: 92020: 92021: 132022: 12023: 102024: 92025: 2
2007high 19 (2018) · low 0 (2007)2025

MAUDE reports naming product code HCH, 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
20071—00
20081—00
20092—00
20100—04
20110—00
20120—04
20130—23
20141—013
20150—09
20160—05
20170—01
20180—019
20191—09
20200—09
20210—013
20221—01
20230—010
20240—09
20250—02
20260—0—

What is it indicated for?

Occlusion of small vessels as a compliment to bipolar coagulation.

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. “K960037: Sugita Avm Microclip.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K960037

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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