510(k) Report

510(k) · Cleared

Cleared

Arthrex Mini Hip PushLock

K201786510(k) SpecialCleared Jul 30, 202030-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 Jul 30, 2020 as substantially equivalent to K151092 (Arthrex, Inc., 2016) after a 30-day review. Its family tree reaches back 9 generations to 1996. 5 later devices descend from it.

Decided
Jul 30, 2020
Review
30 days
Class
Class II
Product code
MAI
Recalls
None
Predicates
1

Its longest line of descent runs back 9 generations to K961555 (1996). 13 ancestors in all. 5 later devices descend from it, 3 citing it directly.

  1. Root · 9 generations backK961555 Acufex Tag Bioabsorbable AnchorsAcufex Microsurgical, Inc. · 1996
  2. 5 generations between
  3. 3 generations backK110660 Arthrex Biocomposite SuturetakArthrex, Inc. · 2011
  4. 2 generations backK140855 Arthrex Suturetak Suture AnchorsArthrex, Inc. · 2014
  5. 1 generation backK151092 Arthrex Short Suture AnchorsArthrex, Inc. · 2016
  6. This deviceK201786 Arthrex Mini Hip PushLockArthrex, Inc. · 2020
  7. Descendant · cites it directly · 1 of its ownK253931 Arthrex Bioabsorbable PushLock Suture AnchorsArthrex, Inc. · 2026
  8. Descendant · cites it directly · 1 of its ownK212381 VersaTap, VersaLat, DueLock, VersaTi, MiniTiOrtho-Design (Pty), Ltd. · 2021
  9. Descendant · 2 generations on · 0 of its ownK262357 Arthrex Bioabsorbable PushLock Suture AnchorsArthrex, Inc. · 2026
  10. Descendant · cites it directly · 0 of its ownK250544 Knotilus+ Biocomposite Knotless AnchorStryker Endoscopy · 2025
  11. Descendant · 2 generations on · 0 of its ownK242296 VersaTap™ Suture Anchor (ADP050); VersaPEEK™ Suture Anchor (APP002)…Ortho-Design (Pty), Ltd. · 2024
Show all 9 generations
  1. Root · 9 generations backK961555 Acufex Tag Bioabsorbable AnchorsAcufex Microsurgical, Inc. · 1996
  2. 8 generations backK031685 Tag Rod Bioraptor Suture Anchor 7209317, 7209318Smith & Nephew, Inc. · 2003 · Recalled
  3. 7 generations backK053344 Bioraptor Suture Anchor, Twinfix 2.8 MM Suture Anchor, Twinfix 3.5…Smith & Nephew, Inc. · 2006
  4. 6 generations backK061863 Arthrex Corkscrew Suture Anchor, Tak, and Pushlock FamilyArthrex, Inc. · 2006
  5. 5 generations backK071177 Arthrex Bio- Composite Suture Anchors: Bio-Composite Pushlock…Arthrex, Inc. · 2007
  6. 4 generations backK091844 Arthrex Bio-Composite Suturetak AnchorsArthrex, Inc. · 2009
  7. 3 generations backK110660 Arthrex Biocomposite SuturetakArthrex, Inc. · 2011
  8. 2 generations backK140855 Arthrex Suturetak Suture AnchorsArthrex, Inc. · 2014
  9. 1 generation backK151092 Arthrex Short Suture AnchorsArthrex, Inc. · 2016
  10. This deviceK201786 Arthrex Mini Hip PushLockArthrex, Inc. · 2020

Most influential descendants

Showing 5 of 5 · See all
  • K253931Arthrex Bioabsorbable PushLock Suture AnchorsArthrex, Inc. · 2026 · cites it directly1descendant
  • K212381VersaTap, VersaLat, DueLock, VersaTi, MiniTiOrtho-Design (Pty), Ltd. · 2021 · cites it directly1descendant
  • K262357Arthrex Bioabsorbable PushLock Suture AnchorsArthrex, Inc. · 2026 · 2 generations on0descendants
  • K250544Knotilus+ Biocomposite Knotless AnchorStryker Endoscopy · 2025 · cites it directly0descendants
  • K242296VersaTap™ Suture Anchor (ADP050); VersaPEEK™ Suture Anchor (APP002); MicroTi™ Suture…Ortho-Design (Pty), Ltd. · 2024 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K961555Acufex Tag Bioabsorbable AnchorsAcufex Microsurgical, Inc.1996—
−8K031685Tag Rod Bioraptor Suture Anchor 7209317, 7209318Smith & Nephew, Inc.20035
−7K053344Bioraptor Suture Anchor, Twinfix 2.8 MM Suture Anchor, Twinfix 3.5 MM Suture…Smith & Nephew, Inc.2006—
−6K061863Arthrex Corkscrew Suture Anchor, Tak, and Pushlock FamilyArthrex, Inc.2006—
−5K071177Arthrex Bio- Composite Suture Anchors: Bio-Composite Pushlock, Bio-Composite…Arthrex, Inc.2007—
−4K091844Arthrex Bio-Composite Suturetak AnchorsArthrex, Inc.2009—
−3K110660Arthrex Biocomposite SuturetakArthrex, Inc.2011—
−2K140855Arthrex Suturetak Suture AnchorsArthrex, Inc.2014—
−1K151092Arthrex Short Suture AnchorsArthrex, Inc.2016—
0 (this device)K201786Arthrex Mini Hip PushLockArthrex, Inc.2020—
+1K253931Arthrex Bioabsorbable PushLock Suture AnchorsArthrex, Inc.2026—
+1K212381VersaTap, VersaLat, DueLock, VersaTi, MiniTiOrtho-Design (Pty), Ltd.2021—
+2K262357Arthrex Bioabsorbable PushLock Suture AnchorsArthrex, Inc.2026—
+1K250544Knotilus+ Biocomposite Knotless AnchorStryker Endoscopy2025—
+2K242296VersaTap™ Suture Anchor (ADP050); VersaPEEK™ Suture Anchor (APP002); MicroTi™…Ortho-Design (Pty), Ltd.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199810
200510
200610
201110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202110
202410
202510
202620
FIG. 1 — Lineage of K201786, 1996–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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
*K151092Arthrex Short Suture Anchors
Summary page 4
…accessories 21 CFR 888.3040: Smooth or threaded metallic bone fastener Regulatory Class II Predicate Device K151092: Arthrex Short Suture Anchors Reference ĞǀŝĐĞ K101679: Arthrex PushLock Purpose of Submission This Special 510(k) p…
Arthrex, Inc.2016—
†K101679Arthrex Pushlock AnchorsArthrex, Inc.2010—

Also cleared against K151092: 4 other devices →

What descends from it? (5)

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

NumberDeviceApplicantDecidedDescendants
K253931Arthrex Bioabsorbable PushLock Suture AnchorsArthrex, Inc.20261
K212381VersaTap, VersaLat, DueLock, VersaTi, MiniTiOrtho-Design (Pty), Ltd.20211
K250544Knotilus+ Biocomposite Knotless AnchorStryker Endoscopy20250

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 24 years and passes through 3 companies; a new generation was cleared every 2.2 years on median.
  • 2 of the 13 ancestors have a recall of any class.
  • Of its descendants, K253931 (Arthrex, Inc., 2026) has gone furthest, with 1 descendant of its own.
  • 4 other devices also cite its predicate K151092.

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. 2020, 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 Mini Hip PushLock is intended to be used for suture (soft tissue) to bone in the hip. Specifically, Acetabular Labral Repair.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K201786: Arthrex Mini Hip PushLock.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K201786

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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