510(k) · Cleared
ClearedGrappler Suture Anchor PCFD Tether System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Paragon 28, Inc. · MBI Fastener, Fixation, Nondegradable, Soft Tissue
Cleared on Mar 17, 2026 as substantially equivalent to K240594 (Paragon 28, Inc., 2024) and 2 other predicates after a 103-day review. Its family tree reaches back 14 generations to 1997.
- Decided
- Mar 17, 2026
- Review
- 103 days
- Class
- Class II
- Product code
- MBI
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 14 generations to K971358 (1997). 123 ancestors in all, the oldest K792022 (1979). No later device cites it as a predicate yet.
- Root · 14 generations backK971358 Bio-Interference Screw, 7 MM, 8 MM, 9 MMArthrex, Inc. · 1997
- 10 generations between
- 3 generations backK222091 Grappler Suture Anchor SystemParagon 28, Inc. · 2022
- 2 generations backK223589 Grappler Suture Anchor R3FLEX IOL SystemParagon 28, Inc. · 2023
- 1 generation backK240594 Grappler Suture Anchor R3FLEX IOL SystemParagon 28, Inc. · 2024
- This deviceK253886 Grappler Suture Anchor PCFD Tether SystemParagon 28, Inc. · 2026
Show all 14 generations
- Root · 14 generations backK971358 Bio-Interference Screw, 7 MM, 8 MM, 9 MMArthrex, Inc. · 1997
- 13 generations backK990454 Bio-Interference ScrewInnovasive Devices, Inc. · 1999
- 12 generations backK993975 Absolute Absorbable Interference ScrewInnovasive Devices, Inc. · 1999
- 11 generations backK013572 Mitek Biocryl Interference ScrewsMitek Products · 2002
- 10 generations backK032717 Biocryl Rapide Interference ScrewMitek Worldwide · 2004
- 9 generations backK060830 Milagro Interference ScrewDepuy Mitek, A Johnson & Johnson Company · 2006
- 8 generations backK073412 Gryphon BR and Healix BR AnchorsDepuy Mitek, A Johnson & Johnson Company · 2008 · Recalled
- 7 generations backK090124 Gryphon P BR DS Anchor W/Orthocord,Gryphon P BR Anchor W/Orthocord…Depuy Mitek, A Johnson & Johnson Company · 2009 · Recalled
- 6 generations backK100012 Gryphon T BR DS Anchor W/Orthocord, Gryphon T BR Anchor W…Depuy Mitek, A Johnson & Johnson Company · 2010
- 5 generations backK102298 Transtend BR Anchor W/ Orthocord, Transtend TI Anchor W/Orthocord…Depuy Mitek, A Johnson & Johnson Company · 2011
- 4 generations backK211002 Grappler Suture Anchor SystemParagon 28, Inc. · 2021 · Recalled
- 3 generations backK222091 Grappler Suture Anchor SystemParagon 28, Inc. · 2022
- 2 generations backK223589 Grappler Suture Anchor R3FLEX IOL SystemParagon 28, Inc. · 2023
- 1 generation backK240594 Grappler Suture Anchor R3FLEX IOL SystemParagon 28, Inc. · 2024
- This deviceK253886 Grappler Suture Anchor PCFD Tether SystemParagon 28, Inc. · 2026
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −14 | K971358 | Bio-Interference Screw, 7 MM, 8 MM, 9 MM | Arthrex, Inc. | 1997 | — |
| −13 | K990454 | Bio-Interference Screw | Innovasive Devices, Inc. | 1999 | — |
| −12 | K993975 | Absolute Absorbable Interference Screw | Innovasive Devices, Inc. | 1999 | — |
| −11 | K013572 | Mitek Biocryl Interference Screws | Mitek Products | 2002 | — |
| −10 | K032717 | Biocryl Rapide Interference Screw | Mitek Worldwide | 2004 | — |
| −9 | K060830 | Milagro Interference Screw | Depuy Mitek, A Johnson & Johnson Company | 2006 | — |
| −8 | K073412 | Gryphon BR and Healix BR Anchors | Depuy Mitek, A Johnson & Johnson Company | 2008 | 1 |
| −7 | K090124 | Gryphon P BR DS Anchor W/Orthocord,Gryphon P BR Anchor W/Orthocord, Model… | Depuy Mitek, A Johnson & Johnson Company | 2009 | 2 |
| −6 | K100012 | Gryphon T BR DS Anchor W/Orthocord, Gryphon T BR Anchor W /Orthocord, Gryphon… | Depuy Mitek, A Johnson & Johnson Company | 2010 | — |
| −5 | K102298 | Transtend BR Anchor W/ Orthocord, Transtend TI Anchor W/Orthocord, Transtend… | Depuy Mitek, A Johnson & Johnson Company | 2011 | — |
| −4 | K211002 | Grappler Suture Anchor System | Paragon 28, Inc. | 2021 | 1 |
| −3 | K222091 | Grappler Suture Anchor System | Paragon 28, Inc. | 2022 | — |
| −2 | K223589 | Grappler Suture Anchor R3FLEX IOL System | Paragon 28, Inc. | 2023 | — |
| −1 | K240594 | Grappler Suture Anchor R3FLEX IOL System | Paragon 28, Inc. | 2024 | — |
| 0 (this device) | K253886 | Grappler Suture Anchor PCFD Tether System | Paragon 28, Inc. | 2026 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1979 | 1 | 0 |
| 1982 | 1 | 0 |
| 1990 | 2 | 0 |
| 1992 | 1 | 0 |
| 1993 | 2 | 0 |
| 1994 | 3 | 0 |
| 1995 | 4 | 0 |
| 1996 | 9 | 0 |
| 1997 | 5 | 0 |
| 1998 | 6 | 0 |
| 1999 | 6 | 0 |
| 2000 | 5 | 0 |
| 2001 | 12 | 0 |
| 2002 | 4 | 0 |
| 2003 | 4 | 0 |
| 2004 | 12 | 0 |
| 2005 | 5 | 0 |
| 2006 | 7 | 0 |
| 2007 | 5 | 0 |
| 2008 | 3 | 0 |
| 2009 | 1 | 0 |
| 2010 | 1 | 0 |
| 2011 | 2 | 0 |
| 2013 | 1 | 0 |
| 2017 | 2 | 0 |
| 2019 | 2 | 0 |
| 2020 | 1 | 0 |
| 2021 | 1 | 0 |
| 2024 | 1 | 0 |
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 K203268 Arthrex FiberTak Suture Anchorscore 21.4 · 11 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (3)
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K240594 | Grappler Suture Anchor R3FLEX IOL SystemSummary page 6…rter handles. Device specific drill guides are provided for tunnel creation. Predicate Device: Grappler Suture Anchor R3FLEX IOL System (K240594) Additional Predicate Device: Grappler Interference Screw System (K241864) Additional Predicate Grappler Sut… | 2024 |
| * | K241864 | Grappler Interference Screw SystemSummary page 6…eation. Predicate Device: Grappler Suture Anchor R3FLEX IOL System (K240594) Additional Predicate Device: Grappler Interference Screw System (K241864) Additional Predicate Grappler Suture Anchor System (K211002) Device: Substantial The proposed Grappler Suture Anchor P… | 2024 |
| * | K211002 | Grappler Suture Anchor SystemSummary page 6…X IOL System (K240594) Additional Predicate Device: Grappler Interference Screw System (K241864) Additional Predicate Grappler Suture Anchor System (K211002) Device: Substantial The proposed Grappler Suture Anchor PCFD Tether System Equivalence: are substantially equiv… | 2021 |
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 29 years and passes through 6 companies; a new generation was cleared every 1.6 years on median.
- 22 of the 123 ancestors have a recall of any class.
How does its category compare?
All MBI devicesMBI 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
2026 to Oct 25, outlined.
Median 510(k) review, days · MBI
58in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · MBI
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · MBI
3,826in 2025
MAUDE reports naming product code MBI, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 16 | 80 | 24 | 240 |
| 2008 | 10 | 69 | 6 | 338 |
| 2009 | 19 | 82 | 2 | 355 |
| 2010 | 17 | 76 | 3 | 291 |
| 2011 | 30 | 75 | 23 | 328 |
| 2012 | 24 | 94 | 6 | 371 |
| 2013 | 31 | 100 | 2 | 442 |
| 2014 | 23 | 101 | 0 | 504 |
| 2015 | 23 | 85 | 0 | 507 |
| 2016 | 17 | 94 | 0 | 795 |
| 2017 | 17 | 70 | 4 | 675 |
| 2018 | 16 | 91 | 2 | 1,072 |
| 2019 | 31 | 90 | 0 | 1,303 |
| 2020 | 35 | 83 | 1 | 1,454 |
| 2021 | 18 | 107 | 0 | 1,890 |
| 2022 | 19 | 64 | 0 | 1,591 |
| 2023 | 52 | 57 | 1 | 2,503 |
| 2024 | 22 | 30 | 1 | 3,779 |
| 2025 | 27 | 58 | 1 | 3,826 |
| 2026 | 30 | 63 | 0 | — |
What is it indicated for?
The Grappler Suture Anchor PCFD Tether System is intended for the fixation of soft tissue to bone including:
Foot/Ankle: Medial Stabilization (Deltoid and Spring Ligament Repair for addressing Progressive Collapsing Foot Deformity), Hindfoot Repair (Correction of Peritalar Subluxation/Dislocation, Hindfoot Valgus Deformity or Subfibular Impingement for Addressing Progressive Collapsing Foot Deformity), Interosseous Talocalcaneal Ligament Repair to address Progressive Collapsing Flatfoot Deformity
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K253886 · printed Nov 6, 2026
Cite this page
510(k) Report. “K253886: Grappler Suture Anchor PCFD Tether System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K253886
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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