510(k) · Cleared
ClearedCoLink Mfx Implant System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
In2bones USA, LLC · HRS Plate, Fixation, Bone
Cleared on Mar 12, 2021 as substantially equivalent to K163293 (In2bones USA, LLC, 2017) and 2 other predicates after a 60-day review. Its family tree reaches back 16 generations to 1996. 1 later device descends from it.
- Decided
- Mar 12, 2021
- Review
- 60 days
- Class
- Class II
- Product code
- HRS
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 16 generations to K962616 (1996). 149 ancestors in all, the oldest K792022 (1979). 1 later device descends from it, 1 citing it directly.
- Root · 16 generations backK962616 Synthes Dorsal Distal Radius Plate (DDRP) SystemSynthes (Usa) · 1996
- 12 generations between
- 3 generations backK143385 Acumed Ankle Plating SystemAcumed, LLC · 2015
- 2 generations backK151886 Acumed Ankle and Small Fragment Base Set UpdateAcumed, LLC · 2015
- 1 generation backK181113 CoLink™ Afx Plating SystemIn2bones USA, LLC · 2018
- This deviceK210060 CoLink Mfx Implant SystemIn2bones USA, LLC · 2021
- Descendant · cites it directly · 0 of its ownK261154 CoLink® & CoLag® Non-Sterile ScrewsIn2Bones USA, LLC · 2026
Show all 16 generations
- Root · 16 generations backK962616 Synthes Dorsal Distal Radius Plate (DDRP) SystemSynthes (Usa) · 1996
- 15 generations backK982732 Synthes (Usa) Distal Radius Plate System (DRPS)Synthes · 1998
- 14 generations backK023007 Distal Radius Fracture Repair SystemHand Innovations, Inc. · 2002
- 13 generations backK030198 Hand Innovations, Inc. Distal Radius Fracture Repair SystemHand Innovations, Inc. · 2003
- 12 generations backK032705 Distal Radius Fracture Repair SystemHand Innovations, Inc. · 2003
- 11 generations backK050932 Distal Volar Radius Anatomical Plate SystemHand Innovations, Inc. · 2005 · Recalled
- 10 generations backK051735 Peri-Loc Locking Bone Plates and Locking Bone Screws for the Upper…Smith & Nephew, Inc. · 2005
- 9 generations backK071563 Peri-Loc Periarticular Locked Plating SystemSmith & Nephew, Inc. · 2007
- 8 generations backK090675 Smith & Nephew, Inc. VLP Foot Plating, Screw System and AccessoriesSmith & Nephew, Inc. · 2009
- 7 generations backK100776 Synthes 2.4 MM/2.7 MM Variable Angle LCP Forefoot/Midfoot SystemSynthes (Usa) · 2010
- 6 generations backK120070 Synthes Variable Angle LCP Elbow SystemSynthes USA · 2012 · Recalled
- 5 generations backK120717 Synthes Variable Angle LCP Elbow System (Medical and Posterolateral…Synthes USA · 2012
- 4 generations backK120854 Synthes VA LCP Ankle Trauma SystemSynthes USA · 2012
- 3 generations backK143385 Acumed Ankle Plating SystemAcumed, LLC · 2015
- 2 generations backK151886 Acumed Ankle and Small Fragment Base Set UpdateAcumed, LLC · 2015
- 1 generation backK181113 CoLink™ Afx Plating SystemIn2bones USA, LLC · 2018
- This deviceK210060 CoLink Mfx Implant SystemIn2bones USA, LLC · 2021
Most influential descendants
Showing 1 of 1 · See all- K261154CoLink® & CoLag® Non-Sterile ScrewsIn2Bones USA, LLC · 2026 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −16 | K962616 | Synthes Dorsal Distal Radius Plate (DDRP) System | Synthes (Usa) | 1996 | — |
| −15 | K982732 | Synthes (Usa) Distal Radius Plate System (DRPS) | Synthes | 1998 | — |
| −14 | K023007 | Distal Radius Fracture Repair System | Hand Innovations, Inc. | 2002 | — |
| −13 | K030198 | Hand Innovations, Inc. Distal Radius Fracture Repair System | Hand Innovations, Inc. | 2003 | — |
| −12 | K032705 | Distal Radius Fracture Repair System | Hand Innovations, Inc. | 2003 | — |
| −11 | K050932 | Distal Volar Radius Anatomical Plate System | Hand Innovations, Inc. | 2005 | 1 |
| −10 | K051735 | Peri-Loc Locking Bone Plates and Locking Bone Screws for the Upper Extremity | Smith & Nephew, Inc. | 2005 | — |
| −9 | K071563 | Peri-Loc Periarticular Locked Plating System | Smith & Nephew, Inc. | 2007 | — |
| −8 | K090675 | Smith & Nephew, Inc. VLP Foot Plating, Screw System and Accessories | Smith & Nephew, Inc. | 2009 | — |
| −7 | K100776 | Synthes 2.4 MM/2.7 MM Variable Angle LCP Forefoot/Midfoot System | Synthes (Usa) | 2010 | — |
| −6 | K120070 | Synthes Variable Angle LCP Elbow System | Synthes USA | 2012 | 1 |
| −5 | K120717 | Synthes Variable Angle LCP Elbow System (Medical and Posterolateral Distal… | Synthes USA | 2012 | — |
| −4 | K120854 | Synthes VA LCP Ankle Trauma System | Synthes USA | 2012 | — |
| −3 | K143385 | Acumed Ankle Plating System | Acumed, LLC | 2015 | — |
| −2 | K151886 | Acumed Ankle and Small Fragment Base Set Update | Acumed, LLC | 2015 | — |
| −1 | K181113 | CoLink™ Afx Plating System | In2bones USA, LLC | 2018 | — |
| 0 (this device) | K210060 | CoLink Mfx Implant System | In2bones USA, LLC | 2021 | — |
| +1 | K261154 | CoLink® & CoLag® Non-Sterile Screws | In2Bones USA, LLC | 2026 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1979 | 1 | 0 |
| 1989 | 1 | 0 |
| 1990 | 3 | 0 |
| 1991 | 1 | 0 |
| 1992 | 1 | 0 |
| 1993 | 2 | 0 |
| 1994 | 4 | 0 |
| 1995 | 2 | 0 |
| 1996 | 7 | 0 |
| 1997 | 2 | 0 |
| 1998 | 4 | 0 |
| 1999 | 4 | 0 |
| 2000 | 12 | 0 |
| 2001 | 10 | 0 |
| 2002 | 3 | 0 |
| 2003 | 5 | 0 |
| 2004 | 8 | 0 |
| 2005 | 8 | 0 |
| 2006 | 9 | 0 |
| 2007 | 4 | 0 |
| 2008 | 9 | 0 |
| 2009 | 7 | 0 |
| 2010 | 9 | 0 |
| 2011 | 5 | 0 |
| 2012 | 5 | 0 |
| 2013 | 1 | 0 |
| 2014 | 1 | 0 |
| 2015 | 3 | 0 |
| 2017 | 2 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2026 | 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 HRS? 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 HRS device
- #1 K222465 Tyber Medical Anatomical Plating Systemscore 27.5 · 16 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 |
|---|---|---|---|
| * | K163293 | Colink™ Plating SystemSummary page 5…eared by the FDA: Page 1 of 2 K210060 Primary Predicate • K163293 – CoLink® Plating System Additional Predicates • K181113 – CoLink® Afx Plating System • K152974 – Wright Ortholoc® 3Di Foo… | 2017 |
| * | K181113 | CoLink™ Afx Plating SystemSummary page 5…Page 1 of 2 K210060 Primary Predicate • K163293 – CoLink® Plating System Additional Predicates • K181113 – CoLink® Afx Plating System • K152974 – Wright Ortholoc® 3Di Foot Plating Reconstruction System Reference Device • K20114… | 2018 |
| * | K152974 | ORTHOLOC® 3Di Foot Plating Reconstruction SystemSummary page 5…K210060 Primary Predicate • K163293 – CoLink® Plating System Additional Predicates • K181113 – CoLink® Afx Plating System • K152974 – Wright Ortholoc® 3Di Foot Plating Reconstruction System Reference Device • K201149 – CoLink® Plating System • K180377 –… | 2015 |
| † | K201149 | CoLink Plating System | 2020 |
| † | K180377 | Fracture and Correction System | 2018 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K261154 | CoLink® & CoLag® Non-Sterile Screws | 2026 | 0 |
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 25 years and passes through 7 companies; a new generation was cleared every 1.6 years on median.
- 36 of the 149 ancestors have a recall of any class.
- Of its descendants, K261154 (In2Bones USA, LLC, 2026) has gone furthest, with 0 descendants of its own.
- 13 other devices also cite its predicate K163293.
How does its category compare?
All HRS devicesHRS Plate, Fixation, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.
FDA decisions per year · HRS
54in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · HRS
90in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · HRS
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · HRS
2,306in 2025
MAUDE reports naming product code HRS, 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 | 35 | 63 | 2 | 339 |
| 2008 | 35 | 87 | 11 | 311 |
| 2009 | 47 | 85 | 3 | 435 |
| 2010 | 49 | 100 | 16 | 491 |
| 2011 | 43 | 88 | 5 | 773 |
| 2012 | 59 | 106 | 4 | 1,663 |
| 2013 | 56 | 89 | 11 | 2,643 |
| 2014 | 76 | 57 | 0 | 2,413 |
| 2015 | 56 | 97 | 7 | 3,095 |
| 2016 | 44 | 109 | 5 | 2,276 |
| 2017 | 57 | 122 | 3 | 2,220 |
| 2018 | 40 | 116 | 2 | 2,663 |
| 2019 | 46 | 89 | 25 | 3,359 |
| 2020 | 48 | 88 | 1 | 2,790 |
| 2021 | 40 | 87 | 9 | 2,442 |
| 2022 | 47 | 144 | 3 | 1,700 |
| 2023 | 40 | 120 | 1 | 2,049 |
| 2024 | 54 | 96 | 0 | 1,849 |
| 2025 | 54 | 90 | 1 | 2,306 |
| 2026 | 51 | 82 | 3 | — |
What is it indicated for?
The CoLink® Mfx Plating System is intended for stabilization and fixation of fractures, revision procedures, joint fusion, osteotomies and reconstruction in the midfoot bones of the foot, including repair of Lis Franc injuries, in both pediatric and adult patients.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K210060 · printed Nov 6, 2026
Cite this page
510(k) Report. “K210060: CoLink Mfx Implant System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K210060
Report an extraction error
Are you the manufacturer?
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