510(k) Report

510(k) · Cleared

Cleared

Flexible Cutting Scissors

K760715510(k) TraditionalCleared Oct 21, 197626-day reviewClass I21 CFR 876.4730

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

V. Mueller O.V. Baxter Healthcare Corp. · KOA Surgical Instruments, G-U, Manual (And Accessories)

Cleared on Oct 21, 1976 after a 26-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Oct 21, 1976
Review
26 days
Class
Class I
Product code
KOA
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2018: 1 descendant cleared19801990200020102020
  1. This deviceK760715 Flexible Cutting ScissorsV. Mueller O.V. Baxter Healthcare Corp. · 1976
  2. Descendant · cites it directly · 0 of its ownK182664 FiXcisionAgency For Medical Innovations GmbH · 2018

Most influential descendants

Showing 1 of 1 · See all
  • K182664FiXcisionAgency For Medical Innovations GmbH · 2018 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K760715Flexible Cutting ScissorsV. Mueller O.V. Baxter Healthcare Corp.1976—
+1K182664FiXcisionAgency For Medical Innovations GmbH2018—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201810
FIG. 1 — Lineage of K760715, 1976–2018Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in KOA? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K182664FiXcisionAgency For Medical Innovations GmbH20180

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?

  • Of its descendants, K182664 (Agency For Medical Innovations GmbH, 2018) has gone furthest, with 0 descendants of its own.

How does its category compare?

All KOA devices

KOA Surgical Instruments, G-U, Manual (And Accessories): FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KOA

1in 2018

2018: 1
2007high 1 (2018) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KOA

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

Recalls per year · KOA

No recall names KOA since 2007.

Adverse event reports per year · KOA

3in 2025

2007: 12009: 12013: 12016: 22017: 32018: 32019: 22020: 12021: 12023: 52024: 22025: 3
2007high 5 (2023) · low 0 (2008)2025

MAUDE reports naming product code KOA, 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—01
20080—00
20090—01
20100—00
20110—00
20120—00
20130—01
20140—00
20150—00
20160—02
20170—03
20181—03
20190—02
20200—01
20210—01
20220—00
20230—05
20240—02
20250—03
20260—0—
Cite this page

510(k) Report. “K760715: Flexible Cutting Scissors.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K760715

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026