510(k) Report

510(k) · Cleared

Cleared

Pre-Waxed Needles with Gold Fiduciary Markers

K071550510(k) AbbreviatedCleared Jul 18, 200742-day reviewClass II21 CFR 892.5730

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

Cp Medical · KXK Source, Brachytherapy, Radionuclide

Cleared on Jul 18, 2007 as substantially equivalent to K043117 (Best Medical International, Inc., 2004) after a 42-day review. Its family tree reaches back 1 generation to 2004. 4 later devices descend from it.

Decided
Jul 18, 2007
Review
42 days
Class
Class II
Product code
KXK
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K043117 (2004). 4 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2011: 1 descendant cleared2013: 1 descendant cleared2012: 1 descendant cleared2017: 1 descendant clearedK043117 · Best Radiopaque Strand; Best Radiopaque Marker · Best Medical International, Inc. · 2004200020052010201520202025
Descendants, by generation 1 generation forward: 1 descendant2 generations forward: 2 descendants3 generations forward: 1 descendant K043117 · Best Radiopaque Strand; Best Radiopaque Marker · Best Medical International, Inc. · 20040
  1. Root · 1 generation backK043117 Best Radiopaque Strand; Best Radiopaque MarkerBest Medical International, Inc. · 2004
  2. This deviceK071550 Pre-Waxed Needles with Gold Fiduciary MarkersCp Medical · 2007
  3. Descendant · cites it directly · 3 of its ownK103449 Brachytherapy Needles, RP Sleeve, RP Brachy-Spacer, Gold MakersRiverpoint Medical · 2011
  4. Descendant · 2 generations on · 1 of its ownK131689 Mri MarkerC4 Imaging, LLC · 2013
  5. Descendant · 3 generations on · 0 of its ownK171487 Sirius MRI Marker NSC4 Imaging, LLC · 2017
  6. Descendant · 2 generations on · 0 of its ownK120859 Pre-Loaded Gold Visicoil CK MarkerRadiomed Corporation · 2012

Most influential descendants

Showing 4 of 4 · See all
  • K103449Brachytherapy Needles, RP Sleeve, RP Brachy-Spacer, Gold MakersRiverpoint Medical · 2011 · cites it directly3descendants
  • K131689Mri MarkerC4 Imaging, LLC · 2013 · 2 generations on1descendant
  • K171487Sirius MRI Marker NSC4 Imaging, LLC · 2017 · 3 generations on0descendants
  • K120859Pre-Loaded Gold Visicoil CK MarkerRadiomed Corporation · 2012 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K043117Best Radiopaque Strand; Best Radiopaque MarkerBest Medical International, Inc.2004—
0 (this device)K071550Pre-Waxed Needles with Gold Fiduciary MarkersCp Medical2007—
+1K103449Brachytherapy Needles, RP Sleeve, RP Brachy-Spacer, Gold MakersRiverpoint Medical2011—
+2K131689Mri MarkerC4 Imaging, LLC2013—
+3K171487Sirius MRI Marker NSC4 Imaging, LLC2017—
+2K120859Pre-Loaded Gold Visicoil CK MarkerRadiomed Corporation2012—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201110
201210
201310
201710
FIG. 1 — Lineage of K071550, 2004–2017Source: 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 KXK? 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 KXK device

  1. #1 K242818 IsoSpherescore 10.9 · 5 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
*K043117Best Radiopaque Strand; Best Radiopaque Marker
Summary page 1
…me: Implantable Radiographic Marker (NEU) Device Classification: Class II, 21 CFR 878.4300 Predicate Devices: Best Radiopaque Marker, K043117 Manufacturer: CP Medical 803 NE 25th Ave. P…
Best Medical International, Inc.2004—

What descends from it? (4)

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

NumberDeviceApplicantDecidedDescendants
K103449Brachytherapy Needles, RP Sleeve, RP Brachy-Spacer, Gold MakersRiverpoint Medical20113

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, K103449 (Riverpoint Medical, 2011) has gone furthest, with 3 descendants of its own.

How does its category compare?

All KXK devices

KXK Source, Brachytherapy, Radionuclide: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.

FDA decisions per year · KXK

2in 2025

2007: 52008: 12009: 72010: 12011: 52012: 32013: 32014: 82015: 22016: 42017: 22018: 12019: 22020: 32022: 12023: 12025: 2
2007high 8 (2014) · low 0 (2021)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KXK

158in 2020

2007: 42 days median2009: 63 days median2011: 94 days median2012: 109 days median2013: 127 days median2014: 96 days median2016: 49 days median2020: 158 days median
2007high 158 (2020) · low 42 (2007)2026

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

Recalls per year · KXK

1in 2016

2008: 12011: 12012: 12016: 1
2007high 1 (2008) · low 0 (2007)2026

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

Adverse event reports per year · KXK

7in 2025

2007: 92008: 152009: 102011: 352012: 42013: 292014: 132015: 62016: 402017: 412018: 282019: 102020: 152021: 622022: 262023: 92024: 152025: 7
2007high 62 (2021) · low 0 (2010)2025

MAUDE reports naming product code KXK, 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
200754209
20081—115
2009763010
20101—00
2011594135
2012310914
20133127029
2014896013
20152—06
2016449140
20172—041
20181—028
20192—010
20203158015
20210—062
20221—026
20231—09
20240—015
20252—07
20260—0—

What is it indicated for?

The needles are used for interstitial placement of gold seed markers. Once implanted, the

gold markers serve as localization devices for the purpose of radiation therapy.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K071550: Pre-Waxed Needles with Gold Fiduciary Markers.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K071550

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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