510(k) Report

510(k) · Cleared

Cleared

Contour Knee

K223429510(k) TraditionalCleared Jan 13, 202360-day reviewClass II21 CFR 892.1000

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

Quality Electrodynamics, LLC · MOS Coil, Magnetic Resonance, Specialty

Cleared on Jan 13, 2023 as substantially equivalent to K183111 (Quality Electrodynamics, LLC, 2018) after a 60-day review. Its family tree reaches back 6 generations to 1993. 2 later devices descend from it.

Decided
Jan 13, 2023
Review
60 days
Class
Class II
Product code
MOS
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K933659 (1993). 2 later devices descend from it, 2 citing it directly.

  1. Root · 6 generations backK933659 Model #100GE1500 Lower Extrem Quad Detect Array CoilMedic, Inc. · 1993
  2. 5 generations backK022395 1.5T Scanmed PV ArrayMedic, Inc. · 2002
  3. 4 generations backK140606 1.5T Procure Array Coil, 3.0T Procure Array CoilResonance Innovations, LLC · 2014
  4. 3 generations backK142755 Siemens 3.0 Blanket Array CoilResonance Innovations, LLC · 2014
  5. 2 generations backK173446 Contour 24Quality Electrodynamics, LLC · 2017
  6. 1 generation backK183111 Contour 24Quality Electrodynamics, LLC · 2018
  7. This deviceK223429 Contour KneeQuality Electrodynamics, LLC · 2023
  8. Descendant · cites it directly · 0 of its ownK233652 Contour Hand/Wrist (Q7000232)Quality Electrodynamics · 2024
  9. Descendant · cites it directly · 0 of its ownK233656 Contour ShoulderQuality Electrodynamics · 2024

Most influential descendants

Showing 2 of 2 · See all
  • K233652Contour Hand/Wrist (Q7000232)Quality Electrodynamics · 2024 · cites it directly0descendants
  • K233656Contour ShoulderQuality Electrodynamics · 2024 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K933659Model #100GE1500 Lower Extrem Quad Detect Array CoilMedic, Inc.1993—
−5K0223951.5T Scanmed PV ArrayMedic, Inc.2002—
−4K1406061.5T Procure Array Coil, 3.0T Procure Array CoilResonance Innovations, LLC2014—
−3K142755Siemens 3.0 Blanket Array CoilResonance Innovations, LLC2014—
−2K173446Contour 24Quality Electrodynamics, LLC2017—
−1K183111Contour 24Quality Electrodynamics, LLC2018—
0 (this device)K223429Contour KneeQuality Electrodynamics, LLC2023—
+1K233652Contour Hand/Wrist (Q7000232)Quality Electrodynamics2024—
+1K233656Contour ShoulderQuality Electrodynamics2024—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202420
FIG. 1 — Lineage of K223429, 1993–2024Source: 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 MOS? 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 MOS device

  1. #1 K253738 3.0T Air 32CH Hnascore 15.2 · 16 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 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
*K183111Contour 24
Summary page 4
…ber 892.1000 Product Code MOS | Legally Marketed Predicate Devices 21 CFR 807.92(a)(3) Predicate # Predicate Trade Name (Primary Predicate is listed first) Product Code K183111 Contour 24 MOS Device Description Summary 21 CFR 807.92(a)(4) The Contour Knee is a receive-only, 12-channel phased array coil d…
Quality Electrodynamics, LLC2018—

What descends from it? (2)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K233652Contour Hand/Wrist (Q7000232)Quality Electrodynamics20240
K233656Contour ShoulderQuality Electrodynamics20240

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 30 years and passes through 3 companies; a new generation was cleared every 4.1 years on median.
  • None of the 6 ancestors has a recall.
  • Of its descendants, K233652 (Quality Electrodynamics, 2024) has gone furthest, with 0 descendants of its own.

How does its category compare?

All MOS devices

MOS Coil, Magnetic Resonance, Specialty: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · MOS

3in 2025

2007: 162008: 192009: 102010: 162011: 252012: 152013: 72014: 122015: 62016: 112017: 92018: 102019: 32020: 52021: 42022: 112023: 102024: 102025: 32026 (partial year): 10
2007high 25 (2011) · low 3 (2019)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MOS

59in 2025

2007: 19 days median2008: 33 days median2009: 43 days median2010: 78 days median2011: 57 days median2012: 49 days median2013: 87 days median2014: 60 days median2015: 58 days median2016: 42 days median2017: 63 days median2018: 30 days median2019: 178 days median2020: 51 days median2021: 41 days median2022: 79 days median2023: 59 days median2024: 39 days median2025: 59 days median2026 (partial year): 45 days median
2007high 178 (2019) · low 19 (2007)2026

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

Recalls per year · MOS

13in 2024

2008: 22010: 12012: 12015: 22019: 82020: 12024: 13
2007high 13 (2024) · low 0 (2007)2026

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

Adverse event reports per year · MOS

2in 2025

2007: 42008: 22009: 52010: 132011: 72012: 122013: 102014: 42015: 52016: 72017: 92018: 72019: 82020: 22021: 32022: 52023: 42024: 82025: 2
2007high 13 (2010) · low 2 (2008)2025

MAUDE reports naming product code MOS, 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
2007161904
2008193322
2009104305
20101678113
2011255707
20121549112
2013787010
2014126004
201565825
2016114207
201796309
2018103007
2019317888
202055112
202144103
2022117905
2023105904
20241039138
202535902
202610450—

What is it indicated for?

The Contour Knee is intended for use with Siemens 0.55T MR systems to produce diagnostic images of knee anatomy that can be interpreted by a trained physician.

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. “K223429: Contour Knee.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K223429

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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