510(k) Report

510(k) · Cleared

Cleared

Milagro Interference Screws

K120589510(k) TraditionalCleared Apr 24, 201256-day reviewClass II21 CFR 888.3030

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

Depuy Mitek, A Johnson & Johnson Company · MAI Fastener, Fixation, Biodegradable, Soft Tissue

Cleared on Apr 24, 2012 as substantially equivalent to K103831 (Depuy Mitek, A Johnson & Johnson Company, 2011) and 4 other predicates after a 56-day review. Its family tree reaches back 9 generations to 1994. 1 later device descends from it.

Decided
Apr 24, 2012
Review
56 days
Class
Class II
Product code
MAI
Recalls
None
Predicates
7

Its longest line of descent runs back 9 generations to K933738 (1994). 43 ancestors in all, the oldest K895711 (1990). 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2011: 1 other ancestor2006: 1 other ancestor2005: 1 other ancestor2004: 2 other ancestors2007: 1 other ancestor2002: 2 other ancestors2001: 3 other ancestors2000: 2 other ancestors1999: 4 other ancestors1998: 4 other ancestors1995: 4 other ancestors1994: 2 other ancestors1997: 1 other ancestor1996: 5 other ancestors1990: 1 other ancestor2012: 1 descendant clearedK933738 · M. Kurosaka Interference Fixation Screw · Depuy, Inc. · 1994 · recalledK955733 · Hyloc Interference Screw (Cannulated)/(Non-Cannulated) · Depuy, Inc. · 1996×3: 3 generations cleared close together, K980440 (1998), K981670 (1998), K982662 (1998) K993073 · Smart Screw Acl Models 237020, 237025, 237030, 238020, 238025, 238030, 239020, 239025, 239030 · Bionx Implants, Ltd. · 1999K032894 · Osteo Acl Screw Model;237020T, 237025T, 237030T, 238020T, 238025T, 238030T, 239020T, 239025T, 239030T, 231020T, 231025T, · Linvatec Biomaterials, Inc. · 2004K052080 · Matryx Interference Screw · Linvatec Biomaterials, Inc. · 2005K102410 · Matryx Interference Screw (5.0-6.5MM) · Conmed Linvatec · 20101990200020102020
  1. Root · 9 generations backK933738 M. Kurosaka Interference Fixation ScrewDepuy, Inc. · 1994 · Recalled
  2. 5 generations between
  3. 3 generations backK032894 Osteo Acl Screw Model;237020T, 237025T, 237030T, 238020T, 238025T…Linvatec Biomaterials, Inc. · 2004
  4. 2 generations backK052080 Matryx Interference ScrewLinvatec Biomaterials, Inc. · 2005
  5. 1 generation backK102410 Matryx Interference Screw (5.0-6.5MM)Conmed Linvatec · 2010
  6. This deviceK120589 Milagro Interference ScrewsDepuy Mitek, A Johnson & Johnson Company · 2012
  7. Descendant · cites it directly · 0 of its ownK122869 Milagro Interference ScrewsDepuy Mitek, A Johnson & Johnson Company · 2012
Show all 9 generations
  1. Root · 9 generations backK933738 M. Kurosaka Interference Fixation ScrewDepuy, Inc. · 1994 · Recalled
  2. 8 generations backK955733 Hyloc Interference Screw (Cannulated)/(Non-Cannulated)Depuy, Inc. · 1996
  3. 7 generations backK980440 Depuy Orthotech Phantom Sof-Thread Soft Tissue Interference ScrewDepuy, Inc. · 1998
  4. 6 generations backK981670 Depuy Profile Round Head Interference Screw and Depuy Phantom…Depuy, Inc. · 1998
  5. 5 generations backK982662 Depuy Profile Round Head Interference Screw, Depuy Phantom…DePuy Orthopaedics, Inc. · 1998 · Recalled
  6. 4 generations backK993073 Smart Screw Acl Models 237020, 237025, 237030, 238020, 238025…Bionx Implants, Ltd. · 1999
  7. 3 generations backK032894 Osteo Acl Screw Model;237020T, 237025T, 237030T, 238020T, 238025T…Linvatec Biomaterials, Inc. · 2004
  8. 2 generations backK052080 Matryx Interference ScrewLinvatec Biomaterials, Inc. · 2005
  9. 1 generation backK102410 Matryx Interference Screw (5.0-6.5MM)Conmed Linvatec · 2010
  10. This deviceK120589 Milagro Interference ScrewsDepuy Mitek, A Johnson & Johnson Company · 2012

Most influential descendants

Showing 1 of 1 · See all
  • K122869Milagro Interference ScrewsDepuy Mitek, A Johnson & Johnson Company · 2012 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K933738M. Kurosaka Interference Fixation ScrewDepuy, Inc.19942
−8K955733Hyloc Interference Screw (Cannulated)/(Non-Cannulated)Depuy, Inc.1996—
−7K980440Depuy Orthotech Phantom Sof-Thread Soft Tissue Interference ScrewDepuy, Inc.1998—
−6K981670Depuy Profile Round Head Interference Screw and Depuy Phantom Resorbable…Depuy, Inc.1998—
−5K982662Depuy Profile Round Head Interference Screw, Depuy Phantom Resorbable…DePuy Orthopaedics, Inc.19984
−4K993073Smart Screw Acl Models 237020, 237025, 237030, 238020, 238025, 238030, 239020…Bionx Implants, Ltd.1999—
−3K032894Osteo Acl Screw Model;237020T, 237025T, 237030T, 238020T, 238025T, 238030T…Linvatec Biomaterials, Inc.2004—
−2K052080Matryx Interference ScrewLinvatec Biomaterials, Inc.2005—
−1K102410Matryx Interference Screw (5.0-6.5MM)Conmed Linvatec2010—
0 (this device)K120589Milagro Interference ScrewsDepuy Mitek, A Johnson & Johnson Company2012—
+1K122869Milagro Interference ScrewsDepuy Mitek, A Johnson & Johnson Company2012—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199010
199420
199540
199650
199710
199840
199940
200020
200130
200220
200420
200510
200610
200710
201110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201210
FIG. 1 — Lineage of K120589, 1994–2012Source: 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 MAI? 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 MAI device

  1. #1 K203495 Arthrex SwiveLock Anchorscore 35.2 · 11 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? (7)

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; numbers the summary cites that cannot be its predicate are marked – and kept off the family tree.

TypeNumberDeviceApplicantDecidedRecalls
*K103831Depuy Mitek Milagro Interference Screw Model 231803, 231804, 231807, 231809
Summary page 2
…tions of the proposed DePuy Mitek MilagroO Interference Screws are substantially equivalent to the existing DePuy Mitek Milagro® Interference Screws cleared under 510(k) K103831, K060830 and K(032717. Technological characteristics including design construct, packaging and indications are similar to the pre…
Depuy Mitek, A Johnson & Johnson Company2011—
*K060830Milagro Interference Screw
Summary page 2
…the proposed DePuy Mitek MilagroO Interference Screws are substantially equivalent to the existing DePuy Mitek Milagro® Interference Screws cleared under 510(k) K103831, K060830 and K(032717. Technological characteristics including design construct, packaging and indications are similar to the predicate de…
Depuy Mitek, A Johnson & Johnson Company2006—
*K032717Biocryl Rapide Interference Screw
Summary page 1
…erence Screws SUBSTANTIAL EQUIVALENCE The proposed DePuy Mitek Milagro" Interference Screws are substantially equivalent to the following devices. " K(103831, 1060830, 1032717: Milagro Interference Screws " 1(051726,K1(41356,K1(20043: Arthrex Tenodesis Screws " K(102410:…
Mitek Worldwide2004—
*K051726Arthrex Tenodesis Family
Summary page 1
…posed DePuy Mitek Milagro" Interference Screws are substantially equivalent to the following devices. " K(103831, 1060830, 1032717: Milagro Interference Screws " 1(051726,K1(41356,K1(20043: Arthrex Tenodesis Screws " K(102410: Linvatec's Matryx Screws FDA PRODUCT CODE…
Arthrex, Inc.2005—
Kept off the family treeK041356FDA’s K041356 is Arthrex Tenodesis Screw Family
Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree
Arthrex, Inc.2004—
Kept off the family treeK020043FDA’s K020043 is 4.0 MM Arthrex Bio-Tendoesis Screw, Model AR-1540B; 5.5 MM Arthrex…
Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree
Arthrex, Inc.2002—
*K102410Matryx Interference Screw (5.0-6.5MM)
Summary page 1
…lly equivalent to the following devices. " K(103831, 1060830, 1032717: Milagro Interference Screws " 1(051726,K1(41356,K1(20043: Arthrex Tenodesis Screws " K(102410: Linvatec's Matryx Screws FDA PRODUCT CODE MAI, I-WC DEVICE CLASSIFICATION This type of fixation screw…
Conmed Linvatec2010—

Also cleared against K103831: 3 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K122869Milagro Interference ScrewsDepuy Mitek, A Johnson & Johnson Company20120

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 18 years and passes through 6 companies; a new generation was cleared every 1.3 years on median.
  • 3 of the 43 ancestors have a recall of any class.
  • Of its descendants, K122869 (Depuy Mitek, A Johnson & Johnson Company, 2012) has gone furthest, with 0 descendants of its own.
  • 3 other devices also cite its predicate K103831.

How does its category compare?

All MAI devices

MAI Fastener, Fixation, Biodegradable, Soft Tissue: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · MAI

8in 2025

2007: 42008: 32009: 92010: 42011: 92012: 62013: 62014: 42015: 52016: 32017: 92018: 132019: 92020: 92021: 82022: 62023: 82024: 72025: 82026 (partial year): 5
2007high 13 (2018) · low 3 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MAI

54in 2025

2007: 100 days median2008: 83 days median2009: 74 days median2010: 122 days median2011: 90 days median2012: 56 days median2013: 135 days median2014: 86 days median2015: 95 days median2016: 191 days median2017: 113 days median2018: 108 days median2019: 41 days median2020: 78 days median2021: 115 days median2022: 136 days median2023: 34 days median2024: 53 days median2025: 54 days median2026 (partial year): 69 days median
2007high 191 (2016) · low 34 (2023)2026

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

Recalls per year · MAI

40in 2020

2011: 52012: 102019: 22020: 402026 (partial year): 1
2007high 40 (2020) · low 0 (2007)2026

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

Adverse event reports per year · MAI

2,148in 2025

2007: 2722008: 1722009: 882010: 892011: 1292012: 1712013: 1662014: 1492015: 1822016: 3012017: 4782018: 1,5902019: 1,2482020: 9572021: 1,2672022: 1,4252023: 1,7182024: 2,3002025: 2,148
2007high 2,300 (2024) · low 88 (2009)2025

MAUDE reports naming product code MAI, 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
200741000272
20083830172
2009974088
20104122089
20119905129
201265610171
201361350166
20144860149
20155950182
201631910301
201791130478
20181310801,590
201994121,248
202097840957
2021811501,267
2022613601,425
202383401,718
202475302,300
202585402,148
20265691—

What is it indicated for?

The Milagro® BR interference screws are designed to attach soft tissues to bone in orthopedic surgical procedures. The screws may be used for interference fixation of soft tissues (such as ligaments or tendons) to bone, when the implant sizes offered are patient appropriate. The implant operates, in conjunction with the appropriate postoperative immobilization, throughout the healing period.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K120589: Milagro Interference Screws.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K120589

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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