510(k) Report

510(k) · Cleared

Cleared

Arthrex SwiveLock Anchor

K192532510(k) SpecialCleared Oct 19, 201933-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

Arthrex, Inc. · MAI Fastener, Fixation, Biodegradable, Soft Tissue

Cleared on Oct 19, 2019 as substantially equivalent to K101823 (Arthrex, Inc., 2011) after a 33-day review. Its family tree reaches back 7 generations to 1996. 16 later devices descend from it.

Decided
Oct 19, 2019
Review
33 days
Class
Class II
Product code
MAI
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K961555 (1996). 9 ancestors in all. 16 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2005: 1 other ancestor1998: 1 other ancestor2023: 3 descendants cleared2020: 1 descendant cleared2021: 2 descendants cleared2022: 1 descendant cleared2026: 4 descendants cleared2025: 3 descendants cleared2024: 2 descendants clearedReference device: K173788 · Arthrex Corkscrew FT · Arthrex, Inc. · 2018Reference device: K180594 · Knotless SutureTak Anchors · Arthrex, Inc. · 2018Reference device: K082810 · Arthrex Bio-Composite Suture Anchors: Arthrex Bio-Composite Pushlock, Bio-Composite Tak and Bio-Composite Corkscrew · Arthrex, Inc. · 2009Reference device: K101679 · Arthrex Pushlock Anchors · Arthrex, Inc. · 2010K961555 · Acufex Tag Bioabsorbable Anchors · Acufex Microsurgical, Inc. · 1996K031685 · Tag Rod Bioraptor Suture Anchor 7209317, 7209318 · Smith & Nephew, Inc. · 2003 · recalledK053344 · Bioraptor Suture Anchor, Twinfix 2.8 MM Suture Anchor, Twinfix 3.5 MM Suture Anchor · Smith & Nephew, Inc. · 2006K061863 · Arthrex Corkscrew Suture Anchor, Tak, and Pushlock Family · Arthrex, Inc. · 2006K071177 · Arthrex Bio- Composite Suture Anchors: Bio-Composite Pushlock, Bio-Composite Tak, Bio-Composite Corkscrew · Arthrex, Inc. · 2007K082810 · Arthrex Bio-Composite Suture Anchors: Arthrex Bio-Composite Pushlock, Bio-Composite Tak and Bio-Composite Corkscrew · Arthrex, Inc. · 2009K101823 · Arthrex Swivelock Anchors · Arthrex, Inc. · 2011 · recalled1995200020052010201520202025
  1. Root · 7 generations backK961555 Acufex Tag Bioabsorbable AnchorsAcufex Microsurgical, Inc. · 1996
  2. 6 generations backK031685 Tag Rod Bioraptor Suture Anchor 7209317, 7209318Smith & Nephew, Inc. · 2003 · Recalled
  3. 5 generations backK053344 Bioraptor Suture Anchor, Twinfix 2.8 MM Suture Anchor, Twinfix 3.5…Smith & Nephew, Inc. · 2006
  4. 4 generations backK061863 Arthrex Corkscrew Suture Anchor, Tak, and Pushlock FamilyArthrex, Inc. · 2006
  5. 3 generations backK071177 Arthrex Bio- Composite Suture Anchors: Bio-Composite Pushlock…Arthrex, Inc. · 2007
  6. 2 generations backK082810 Arthrex Bio-Composite Suture Anchors: Arthrex Bio-Composite…Arthrex, Inc. · 2009
  7. 1 generation backK101823 Arthrex Swivelock AnchorsArthrex, Inc. · 2011 · Recalled
  8. This deviceK192532 Arthrex SwiveLock AnchorArthrex, Inc. · 2019
  9. Descendant · cites it directly · 15 of its ownK201749 Arthrex SwiveLock AnchorArthrex, Inc. · 2020
  10. Descendant · 2 generations on · 13 of its ownK203495 Arthrex SwiveLock AnchorArthrex, Inc. · 2021 · Recalled
  11. Descendant · 3 generations on · 1 of its ownK243712 WasherCap™ Mini Fixation System (Model 45)Abanza Tecnomed S.L · 2025
  12. Descendant · 3 generations on · 1 of its ownK233893 AlphaVent Knotless SP PEEK AnchorStryker Endoscopy · 2024
  13. Descendant · cites it directly · 1 of its ownK230435 Arthrex 3.9 mm SwiveLock AnchorArthrex, Inc. · 2023

Showing 5 of 16 descendants. See all descendants

Descendants cleared per year

2020: 12021: 22022: 12023: 32024: 22025: 32026: 4
2020high 4 (2026) · low 1 (2020)2026

Most influential descendants

Showing 5 of 16 · See all
  • K201749Arthrex SwiveLock AnchorArthrex, Inc. · 2020 · cites it directly15descendants
  • K203495Arthrex SwiveLock AnchorArthrex, Inc. · 2021 · 2 generations on13descendants
  • K243712WasherCap™ Mini Fixation System (Model 45)Abanza Tecnomed S.L · 2025 · 3 generations on1descendant
  • K233893AlphaVent Knotless SP PEEK AnchorStryker Endoscopy · 2024 · 3 generations on1descendant
  • K230435Arthrex 3.9 mm SwiveLock AnchorArthrex, Inc. · 2023 · cites it directly1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K961555Acufex Tag Bioabsorbable AnchorsAcufex Microsurgical, Inc.1996—
−6K031685Tag Rod Bioraptor Suture Anchor 7209317, 7209318Smith & Nephew, Inc.20035
−5K053344Bioraptor Suture Anchor, Twinfix 2.8 MM Suture Anchor, Twinfix 3.5 MM Suture…Smith & Nephew, Inc.2006—
−4K061863Arthrex Corkscrew Suture Anchor, Tak, and Pushlock FamilyArthrex, Inc.2006—
−3K071177Arthrex Bio- Composite Suture Anchors: Bio-Composite Pushlock, Bio-Composite…Arthrex, Inc.2007—
−2K082810Arthrex Bio-Composite Suture Anchors: Arthrex Bio-Composite Pushlock…Arthrex, Inc.2009—
−1K101823Arthrex Swivelock AnchorsArthrex, Inc.20116
0 (this device)K192532Arthrex SwiveLock AnchorArthrex, Inc.2019—
+1K201749Arthrex SwiveLock AnchorArthrex, Inc.2020—
+2K203495Arthrex SwiveLock AnchorArthrex, Inc.20211
+3K243712WasherCap™ Mini Fixation System (Model 45)Abanza Tecnomed S.L2025—
+3K233893AlphaVent Knotless SP PEEK AnchorStryker Endoscopy2024—
+1K230435Arthrex 3.9 mm SwiveLock AnchorArthrex, Inc.2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199810
200510

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
202120
202210
202330
202420
202530
202640
FIG. 1 — Lineage of K192532, 1996–2026Source: 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.

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
Get a 510(k) Report

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
*K101823Arthrex Swivelock Anchors
Summary page 4
…accessories 21 CFR 888.3040: Smooth or threaded metallic bone fixation fastener Regulatory Class Class II Predicate Device K101823: Arthrex SwiveLock Anchors Reference Device K173788: Arthrex Corkscrew FT K180594: Knotless…
Arthrex, Inc.20116
†K173788Arthrex Corkscrew FTArthrex, Inc.2018—
†K180594Knotless SutureTak AnchorsArthrex, Inc.2018—
†K082810Arthrex Bio-Composite Suture Anchors: Arthrex Bio-Composite Pushlock, Bio-Composite Tak…Arthrex, Inc.2009—
†K101679Arthrex Pushlock AnchorsArthrex, Inc.2010—

Also cleared against K101823: 13 other devices →

What descends from it? (16)

See all 16

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

NumberDeviceApplicantDecidedDescendants
K201749Arthrex SwiveLock AnchorArthrex, Inc.202015
K230435Arthrex 3.9 mm SwiveLock AnchorArthrex, Inc.20231

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 23 years and passes through 3 companies; a new generation was cleared every 2.0 years on median.
  • 3 of the 9 ancestors have a recall of any class.
  • Of its descendants, K201749 (Arthrex, Inc., 2020) has gone furthest, with 15 descendants of its own.
  • 13 other devices also cite its predicate K101823.

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. 2019, 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 Arthrex SwiveLock Anchor is intended for fixation of suture (soft tissue) to bone in the shoulder, foot/ankle, knee, hand/wrist, elbow, and hip in the following procedures: • Shoulder: Rotator Cuff Repair, Bankart Repair, SLAP Lesion Repair, Biceps Tenodesis, Acromio-Clavicular Separation Repair, Deltoid Repair, Capsular Shift or Capsulolabral Reconstruction • Foot/Ankle: Lateral Stabilization, Medial Stabilization, Achilles Tendon Repair, Hallux…

Read the full statement (121 words)

The Arthrex SwiveLock Anchor is intended for fixation of suture (soft tissue) to bone in the shoulder, foot/ankle, knee, hand/wrist, elbow, and hip in the following procedures:

• Shoulder: Rotator Cuff Repair, Bankart Repair, SLAP Lesion Repair, Biceps Tenodesis, Acromio-Clavicular Separation Repair, Deltoid Repair, Capsular Shift or Capsulolabral Reconstruction

• Foot/Ankle: Lateral Stabilization, Medial Stabilization, Achilles Tendon Repair, Hallux Valgus reconstruction, Mid-foot reconstruction, Metatarsal Ligament Repair/ Tendon Repair, Bunionectomy

• Knee: Medial Collateral Ligament Repair, Lateral Collateral Ligament Repair, Patellar Tendon Repair, Posterior Oblique Ligament Repair, Iliotibial Band Tenodesis

• Hand/Wrist: Scapholunate Ligament Reconstruction, Ulnar or Radial Collateral Ligament Reconstruction

• Elbow: Biceps Tendon Reattachment, Ulnar or Radial Collateral Ligament Reconstruction, Lateral Epicondylitis Repair

• Hip: Capsular Repair, Acetabular labral repair

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K192532: Arthrex SwiveLock Anchor.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K192532

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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