510(k) Report

510(k) · Cleared

Cleared

Tigon Medical Static Javelin All-Suture Anchors & Javelin All-Suture Anchor Line

K260921510(k) SpecialCleared Apr 21, 202633-day reviewClass II21 CFR 888.3040

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

Tigon Medical · MBI Fastener, Fixation, Nondegradable, Soft Tissue

Cleared on Apr 21, 2026 as substantially equivalent to K252596 (Tigon Medical, 2025) and 3 other predicates after a 33-day review. Its family tree reaches back 11 generations to 1996.

Decided
Apr 21, 2026
Review
33 days
Class
Class II
Product code
MBI
Recalls
None
Predicates
4

Its longest line of descent runs back 11 generations to K961555 (1996). 66 ancestors in all, the oldest K813581 (1982). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2023: 1 other ancestor2019: 1 other ancestor2013: 1 other ancestor2012: 4 other ancestors2011: 2 other ancestors2010: 1 other ancestor2009: 1 other ancestor2008: 2 other ancestors2007: 6 other ancestors2004: 4 other ancestors2006: 1 other ancestor2005: 3 other ancestors2002: 1 other ancestor2001: 8 other ancestors2000: 6 other ancestors1998: 1 other ancestor1999: 1 other ancestor1997: 3 other ancestors1992: 1 other ancestor1982: 1 other ancestor1996: 2 other ancestors1993: 1 other ancestor1995: 1 other ancestor1994: 1 other ancestor1990: 1 other ancestorReference device: K230311 · HyperSuture · Threadstone, LLC · 2023K961555 · 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. · 2009×2: 2 generations cleared close together, K101823 (2011), K110545 (2011) K133671 · Iconix All Suture Anchors · Stryker Corp. · 2014K242529 · Tigon Medical All-Suture Anchors (ASA) · Tigon Medical · 2024K252596 · Tigon Medical Knotless and Dual Javelin All-Suture Anchors · Tigon Medical · 202519801990200020102020
  1. Root · 11 generations backK961555 Acufex Tag Bioabsorbable AnchorsAcufex Microsurgical, Inc. · 1996
  2. 7 generations between
  3. 3 generations backK133671 Iconix All Suture AnchorsStryker Corp. · 2014
  4. 2 generations backK242529 Tigon Medical All-Suture Anchors (ASA)Tigon Medical · 2024
  5. 1 generation backK252596 Tigon Medical Knotless and Dual Javelin All-Suture AnchorsTigon Medical · 2025
  6. This deviceK260921 Tigon Medical Static Javelin All-Suture Anchors & Javelin All-Suture…Tigon Medical · 2026
Show all 11 generations
  1. Root · 11 generations backK961555 Acufex Tag Bioabsorbable AnchorsAcufex Microsurgical, Inc. · 1996
  2. 10 generations backK031685 Tag Rod Bioraptor Suture Anchor 7209317, 7209318Smith & Nephew, Inc. · 2003 · Recalled
  3. 9 generations backK053344 Bioraptor Suture Anchor, Twinfix 2.8 MM Suture Anchor, Twinfix 3.5…Smith & Nephew, Inc. · 2006
  4. 8 generations backK061863 Arthrex Corkscrew Suture Anchor, Tak, and Pushlock FamilyArthrex, Inc. · 2006
  5. 7 generations backK071177 Arthrex Bio- Composite Suture Anchors: Bio-Composite Pushlock…Arthrex, Inc. · 2007
  6. 6 generations backK082810 Arthrex Bio-Composite Suture Anchors: Arthrex Bio-Composite…Arthrex, Inc. · 2009
  7. 5 generations backK101823 Arthrex Swivelock AnchorsArthrex, Inc. · 2011 · Recalled
  8. 4 generations backK110545 Smith & Nephew Next Generation Fully Threaded Peek Suture Anchor…Smith & Nephew, Inc. · 2011
  9. 3 generations backK133671 Iconix All Suture AnchorsStryker Corp. · 2014
  10. 2 generations backK242529 Tigon Medical All-Suture Anchors (ASA)Tigon Medical · 2024
  11. 1 generation backK252596 Tigon Medical Knotless and Dual Javelin All-Suture AnchorsTigon Medical · 2025
  12. This deviceK260921 Tigon Medical Static Javelin All-Suture Anchors & Javelin All-Suture…Tigon Medical · 2026
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−11K961555Acufex Tag Bioabsorbable AnchorsAcufex Microsurgical, Inc.1996—
−10K031685Tag Rod Bioraptor Suture Anchor 7209317, 7209318Smith & Nephew, Inc.20035
−9K053344Bioraptor Suture Anchor, Twinfix 2.8 MM Suture Anchor, Twinfix 3.5 MM Suture…Smith & Nephew, Inc.2006—
−8K061863Arthrex Corkscrew Suture Anchor, Tak, and Pushlock FamilyArthrex, Inc.2006—
−7K071177Arthrex Bio- Composite Suture Anchors: Bio-Composite Pushlock, Bio-Composite…Arthrex, Inc.2007—
−6K082810Arthrex Bio-Composite Suture Anchors: Arthrex Bio-Composite Pushlock…Arthrex, Inc.2009—
−5K101823Arthrex Swivelock AnchorsArthrex, Inc.20116
−4K110545Smith & Nephew Next Generation Fully Threaded Peek Suture Anchor (Ngftsa PK)Smith & Nephew, Inc.2011—
−3K133671Iconix All Suture AnchorsStryker Corp.2014—
−2K242529Tigon Medical All-Suture Anchors (ASA)Tigon Medical2024—
−1K252596Tigon Medical Knotless and Dual Javelin All-Suture AnchorsTigon Medical2025—
0 (this device)K260921Tigon Medical Static Javelin All-Suture Anchors & Javelin All-Suture Anchor LineTigon Medical2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198210
199010
199210
199310
199410
199510
199620
199730
199810
199910
200060
200180
200210
200440
200530
200610
200760
200820
200910
201010
201120
201240
201310
201910
202310
FIG. 1 — Lineage of K260921, 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 MBI? 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 MBI device

  1. #1 K203268 Arthrex FiberTak Suture Anchorscore 21.4 · 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? (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
*K252596Tigon Medical Knotless and Dual Javelin All-Suture Anchors
Summary page 5
…ner Regulatory Class: II Product Code/Panel: MBI Predicate Devices: Tigon Medical Knotless and Dual Javelin All-Suture Anchors (K252596) Additional: Tigon Medical All-Suture Anchors (K242529) Additional: Tigon Medic…
Tigon Medical2025—
*K242529Tigon Medical All-Suture Anchors (ASA)
Summary page 5
…: Tigon Medical Knotless and Dual Javelin All-Suture Anchors (K252596) Additional: Tigon Medical All-Suture Anchors (K242529) Additional: Tigon Medical Tomahawk Anchors, Dual Anchors, Eye-Deal Anchors, Ten…
Tigon Medical2024—
*K220464Tigon Medical Gryphon Anchor Line
Summary page 5
…-Suture Anchors (K242529) Additional: Tigon Medical Tomahawk Anchors, Dual Anchors, Eye-Deal Anchors, Tenodesis Anchors (K220464) Additional: Tigon Medical Tissue Anchors (K182507) Reference: Threadstone Hype…
Tigon Medical2023—
*K182507Tigon Medical Tissue Anchors
Summary page 5
…Tomahawk Anchors, Dual Anchors, Eye-Deal Anchors, Tenodesis Anchors (K220464) Additional: Tigon Medical Tissue Anchors (K182507) Reference: Threadstone HyperSuture (K230311)…
Tigon Medical2019—
†K230311HyperSutureThreadstone, LLC2023—

What descends from it?

No later submission names this one as a predicate yet.

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 30 years and passes through 5 companies; a new generation was cleared every 1.6 years on median.
  • 11 of the 66 ancestors have a recall of any class.

How does its category compare?

All MBI devices

MBI Fastener, Fixation, Nondegradable, Soft Tissue: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, this device’s year, is highlighted.

FDA decisions per year · MBI

27in 2025

2007: 162008: 102009: 192010: 172011: 302012: 242013: 312014: 232015: 232016: 172017: 172018: 162019: 312020: 352021: 182022: 192023: 522024: 222025: 272026 (partial year): 30
2007high 52 (2023) · low 10 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MBI

58in 2025

2007: 80 days median2008: 69 days median2009: 82 days median2010: 76 days median2011: 75 days median2012: 94 days median2013: 100 days median2014: 101 days median2015: 85 days median2016: 94 days median2017: 70 days median2018: 91 days median2019: 90 days median2020: 83 days median2021: 107 days median2022: 64 days median2023: 57 days median2024: 30 days median2025: 58 days median2026 (partial year): 63 days median
2007high 107 (2021) · low 30 (2024)2026

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

Recalls per year · MBI

1in 2025

2007: 242008: 62009: 22010: 32011: 232012: 62013: 22017: 42018: 22020: 12023: 12024: 12025: 1
2007high 24 (2007) · low 0 (2014)2026

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

Adverse event reports per year · MBI

3,826in 2025

2007: 2402008: 3382009: 3552010: 2912011: 3282012: 3712013: 4422014: 5042015: 5072016: 7952017: 6752018: 1,0722019: 1,3032020: 1,4542021: 1,8902022: 1,5912023: 2,5032024: 3,7792025: 3,826
2007high 3,826 (2025) · low 240 (2007)2025

MAUDE reports naming product code MBI, 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
2007168024240
200810696338
200919822355
201017763291
2011307523328
201224946371
2013311002442
2014231010504
201523850507
201617940795
201717704675
2018169121,072
2019319001,303
2020358311,454
20211810701,890
2022196401,591
2023525712,503
2024223013,779
2025275813,826
202630630—

What is it indicated for?

The Tigon Medical All-Suture Anchors are intended for the reattachment of soft tissue to bone for the following indications: • Elbow: Biceps Tendon Reattachment, Ulnar or Radial Collateral Ligament Reconstruction • Shoulder: Rotator Cuff Repair, Bankart Repair, SLAP Lesion Repair, Biceps Tenodesis, Acromio-Clavicular Separation Repair, Deltoid Repair, Capsular Shift or Capsulolabral Repair • Hand/Wrist: Scaphulolunate Ligament Reconstruction, Carpal…

Read the full statement (132 words)

The Tigon Medical All-Suture Anchors are intended for the reattachment of soft tissue to bone for the following indications:

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

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

• Hand/Wrist: Scaphulolunate Ligament Reconstruction, Carpal Ligament Reconstruction, Repair/Reconstruction of Collateral Ligaments, Repair ofFlexor and Extensor Tendons at the PIP, DIP and MCP Joints for all Digits, Digital Tendon Repair

• Foot/Ankle: Lateral Stabilization, Medial Stabilization, Achilles Tendon Repair, Metatarsal Ligament Repair, Hallux Valgus Reconstruction, Digital Tendon Transfers, Mid-foot Reconstruction

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

• Hip: Capsular Repair, Acetabular Labral Repair, Gluteal Tendon Repair

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K260921: Tigon Medical Static Javelin All-Suture Anchors & Javelin All-Suture Anchor Line.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K260921

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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