510(k) Report

510(k) · Cleared

Cleared

Marrow Marxman

K260572510(k) TraditionalCleared Aug 4, 2026166-day reviewClass II21 CFR 876.1075

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

Medimetrix, LLC · KNW Instrument, Biopsy

Cleared on Aug 4, 2026 as substantially equivalent to K223612 (Ranfac Corporation, 2023) and 3 other predicates after a 166-day review. Its family tree reaches back 10 generations to 1987. 1 of the 35 devices in its family, counting itself, has a Class I recall.

Decided
Aug 4, 2026
Review
166 days
Class
Class II
Product code
KNW
Recalls
None
Predicates
4

Its longest line of descent runs back 10 generations to K871390 (1987). 34 ancestors in all. No later device cites it as a predicate yet. 1 of the 35 devices in this family, counting this one, has a Class I recall.

  1. Root · 10 generations backK871390 Bard Biopty Biopsy SystemC.R. Bard, Inc. · 1987
  2. 6 generations between
  3. 3 generations backK140991 Ranfac Aspiration Needle with Adjustable GuideRanfac, Corp. · 2014
  4. 2 generations backK150563 Marrow Cellution Bone Marrow Aspiration NeedleRanfac, Corp. · 2015
  5. 1 generation backK202287 Ran-Flex-B Bone Marrow Aspiration NeedleRanfac Corporation · 2020
  6. This deviceK260572 Marrow MarxmanMedimetrix, LLC · 2026
Show all 10 generations
  1. Root · 10 generations backK871390 Bard Biopty Biopsy SystemC.R. Bard, Inc. · 1987
  2. 9 generations backK962969 Medical Device Technologies, Inc.UltraMedical Device Technologies, Inc. · 1996
  3. 8 generations backK982085 Medical Device Technologies, Inc. Tru-Core Disposale Semi-Automatic…Medical Device Technologies, Inc. · 1998
  4. 7 generations backK982960 Meical Device Technologies, Inc. Tru-Core Disposable Automatic…Medical Device Technologies, Inc. · 1998 · Recalled
  5. 6 generations backK990839 Tru-Core I Reusable Biopsy InstrumentMedical Device Technologies, Inc. · 1999
  6. 5 generations backK051506 Mielo-Can, Best-Lisas, Ben - Bone Biopsy. Fast-Cut, Colt…Sterylab S.R.L. · 2005
  7. 4 generations backK131157 Ranfac Bone Marrow Aspiration NeedleRanfac, Corp. · 2013
  8. 3 generations backK140991 Ranfac Aspiration Needle with Adjustable GuideRanfac, Corp. · 2014
  9. 2 generations backK150563 Marrow Cellution Bone Marrow Aspiration NeedleRanfac, Corp. · 2015
  10. 1 generation backK202287 Ran-Flex-B Bone Marrow Aspiration NeedleRanfac Corporation · 2020
  11. This deviceK260572 Marrow MarxmanMedimetrix, LLC · 2026

Class I recalls in this family

View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−10K871390Bard Biopty Biopsy SystemC.R. Bard, Inc.1987—
−9K962969Medical Device Technologies, Inc.UltraMedical Device Technologies, Inc.1996—
−8K982085Medical Device Technologies, Inc. Tru-Core Disposale Semi-Automatic Biopdy…Medical Device Technologies, Inc.1998—
−7K982960Meical Device Technologies, Inc. Tru-Core Disposable Automatic Biopsy InstrumentMedical Device Technologies, Inc.19982
−6K990839Tru-Core I Reusable Biopsy InstrumentMedical Device Technologies, Inc.1999—
−5K051506Mielo-Can, Best-Lisas, Ben - Bone Biopsy. Fast-Cut, Colt, Spring-Cut, Bio-Cut…Sterylab S.R.L.2005—
−4K131157Ranfac Bone Marrow Aspiration NeedleRanfac, Corp.2013—
−3K140991Ranfac Aspiration Needle with Adjustable GuideRanfac, Corp.2014—
−2K150563Marrow Cellution Bone Marrow Aspiration NeedleRanfac, Corp.2015—
−1K202287Ran-Flex-B Bone Marrow Aspiration NeedleRanfac Corporation2020—
0 (this device)K260572Marrow MarxmanMedimetrix, LLC2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198920
199010
199220
199420
199510
199610
199710
199831
200010
200220
200320
200410
200510
200610
201010
201210
202310
FIG. 1 — Lineage of K260572, 1987–2026Source: 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 KNW device

  1. #1 K240664 ALARA BMA Neuro Access Kit (ALARA BMAN and…score 14.1 · 12 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? (4)

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
*K223612Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA)
Summary page 5
…Panel: Gastroenterology & Urology Product Code: KNW Primary Predicate: Ranfac Lateral Access Bone Marrow Aspiration Needle – K223612 Device Description: The Marrow Marxman is a manual, sterile disposable flexible cannula intended for the purposes of aspiratin…
Ranfac Corporation2023—
*K150563Marrow Cellution Bone Marrow Aspiration Needle
Summary page 6
…Needle (CRVS-BMA-LA) (Ranfac Corporation) – K223612 Additional Predicate Devices: • Marrow Cellution Bone Marrow Aspiration Needle (Ranfac Corporation) – K150563 • Ran-Flex B Bone Marrow Aspiration Needle (Ranfac Corporation) – K202287 • Ranfac Bone Marrow Aspiration Needle (Ran…
Ranfac, Corp.2015—
*K202287Ran-Flex-B Bone Marrow Aspiration Needle
Summary page 6
…e Devices: • Marrow Cellution Bone Marrow Aspiration Needle (Ranfac Corporation) – K150563 • Ran-Flex B Bone Marrow Aspiration Needle (Ranfac Corporation) – K202287 • Ranfac Bone Marrow Aspiration Needle (Ranfac Corporation) – K131157 There are insignificant differences between the subj…
Ranfac Corporation2020—
*K131157Ranfac Bone Marrow Aspiration Needle
Summary page 6
…orporation) – K150563 • Ran-Flex B Bone Marrow Aspiration Needle (Ranfac Corporation) – K202287 • Ranfac Bone Marrow Aspiration Needle (Ranfac Corporation) – K131157 There are insignificant differences between the subject Marrow Marxman and the predicate devices. The Indications for Use are id…
Ranfac, Corp.2013—

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.

  • K980196MD Tech Biopsy Set for Bone and Bone MarrowMedical Device Technologies, Inc. · 1998 · 3 generations back · ◆ in the 1998 ancestors bar of FIG. 13 Class I recalls

What does this lineage say?

  • The line of descent spans 39 years and passes through 6 companies; a new generation was cleared every 5.3 years on median.
  • 5 of the 34 ancestors have a recall of any class; 1 has a Class I recall.

How does its category compare?

All KNW devices

KNW Instrument, Biopsy: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, this device’s year, is highlighted.

FDA decisions per year · KNW

12in 2025

2007: 62008: 42009: 62010: 32011: 102012: 72013: 32014: 82015: 102016: 92017: 82018: 72019: 52020: 82021: 92022: 82023: 72024: 52025: 122026 (partial year): 7
2007high 12 (2025) · low 3 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KNW

178in 2025

2007: 94 days median2008: 53 days median2009: 35 days median2010: 57 days median2011: 64 days median2012: 94 days median2013: 100 days median2014: 95 days median2015: 106 days median2016: 127 days median2017: 90 days median2018: 71 days median2019: 94 days median2020: 92 days median2021: 54 days median2022: 203 days median2023: 164 days median2024: 114 days median2025: 178 days median2026 (partial year): 29 days median
2007high 203 (2022) · low 35 (2009)2026

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

Recalls per year · KNW

1in 2024

2007: 12008: 72009: 32010: 22011: 52012: 12013: 1, 1 Class I2014: 32016: 52017: 12019: 42021: 32022: 32023: 22024: 12026 (partial year): 4, 3 Class I
2007high 7 (2008) · low 0 (2015)2026

Class I (4 since 2007) Class II/III not classified

Adverse event reports per year · KNW

1,667in 2025

2007: 7662008: 3632009: 3512010: 1622011: 672012: 932013: 982014: 1932015: 5912016: 2972017: 7602018: 1,0122019: 4,1952020: 5,1202021: 1,0202022: 5352023: 9312024: 1,2832025: 1,667
2007high 5,120 (2020) · low 67 (2011)2025

MAUDE reports naming product code KNW, 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
20076941766
20084537363
20096353351
20103572162
20111064567
2012794193
201331001 (1)98
20148953193
2015101060591
201691275297
20178901760
201877101,012
201959444,195
202089205,120
202195431,020
202282033535
202371642931
2024511411,283
20251217801,667
20267294 (3)—

What is it indicated for?

The Marrow Marxman is intended for aspiration of bone marrow or autologous blood using a standard piston syringe.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K260572: Marrow Marxman.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K260572

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Record history
  • FDA decision record loaded Oct 30, 2026
  • Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026