510(k) · Cleared
ClearedFootmotion Plating System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Newclip Technics · HRS Plate, Fixation, Bone
Cleared on Jul 1, 2022 as substantially equivalent to K161448 (Newclip Technics, 2016) and 7 other predicates after a 49-day review. Its family tree reaches back 16 generations to 1996.
- Decided
- Jul 1, 2022
- Review
- 49 days
- Class
- Class II
- Product code
- HRS
- Recalls
- None
- Predicates
- 8
Its longest line of descent runs back 16 generations to K962616 (1996). 156 ancestors in all, the oldest K792022 (1979). No later device cites it as a predicate yet.
- Root · 16 generations backK962616 Synthes Dorsal Distal Radius Plate (DDRP) SystemSynthes (Usa) · 1996
- 12 generations between
- 3 generations backK143061 Activ Ankle Locking Plating SystemNewclip Technics · 2015
- 2 generations backK152289 Alians Elbow Locking Plating SystemNewclip Technics · 2016
- 1 generation backK173641 Activ AnkleNewclip Technics · 2018
- This deviceK221395 Footmotion Plating SystemNewclip Technics · 2022
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 backK143061 Activ Ankle Locking Plating SystemNewclip Technics · 2015
- 2 generations backK152289 Alians Elbow Locking Plating SystemNewclip Technics · 2016
- 1 generation backK173641 Activ AnkleNewclip Technics · 2018
- This deviceK221395 Footmotion Plating SystemNewclip Technics · 2022
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 | K143061 | Activ Ankle Locking Plating System | Newclip Technics | 2015 | — |
| −2 | K152289 | Alians Elbow Locking Plating System | Newclip Technics | 2016 | — |
| −1 | K173641 | Activ Ankle | Newclip Technics | 2018 | — |
| 0 (this device) | K221395 | Footmotion Plating System | Newclip Technics | 2022 | — |
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 | 2 | 0 |
| 1993 | 2 | 0 |
| 1994 | 4 | 0 |
| 1995 | 2 | 0 |
| 1996 | 8 | 0 |
| 1997 | 3 | 0 |
| 1998 | 5 | 0 |
| 1999 | 5 | 0 |
| 2000 | 13 | 0 |
| 2001 | 11 | 0 |
| 2002 | 4 | 0 |
| 2003 | 5 | 0 |
| 2004 | 9 | 0 |
| 2005 | 8 | 0 |
| 2006 | 10 | 0 |
| 2007 | 4 | 0 |
| 2008 | 7 | 0 |
| 2009 | 9 | 0 |
| 2010 | 7 | 0 |
| 2011 | 4 | 0 |
| 2012 | 4 | 0 |
| 2013 | 2 | 0 |
| 2015 | 1 | 0 |
| 2016 | 2 | 0 |
| 2017 | 2 | 0 |
| 2019 | 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? (8)
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 |
|---|---|---|---|
| * | K161448 | Footmotion Plating SystemSummary page 5…K221395 Page 2 of 4 3. Primary predicate or legally marketed devices which are substantially equivalent: • Footmotion Plating System of Newclip Technics (K161448 / K171510) Additional predicate or legally marketed devices which are substantially equivalent: • Ortholoc® 3Di Midfoot/Flat… | 2016 |
| * | K171510 | Footmotion Plating SystemSummary page 5…21395 Page 2 of 4 3. Primary predicate or legally marketed devices which are substantially equivalent: • Footmotion Plating System of Newclip Technics (K161448 / K171510) Additional predicate or legally marketed devices which are substantially equivalent: • Ortholoc® 3Di Midfoot/Flatfoot Syste… | 2017 |
| * | K121651 | Ortholoc 3DI Midfoot/Flatfoot SystemSummary page 5…10) Additional predicate or legally marketed devices which are substantially equivalent: • Ortholoc® 3Di Midfoot/Flatfoot System of Wright Medical Technology (K121651), • DARCO Locking Bone Plate System of Wright Medical Technology (K061808), • A.L.P.S Calcaneal Plating System of Bio… | 2012 |
| * | K061808 | Darco Locking Bone Plate SystemSummary page 5…valent: • Ortholoc® 3Di Midfoot/Flatfoot System of Wright Medical Technology (K121651), • DARCO Locking Bone Plate System of Wright Medical Technology (K061808), • A.L.P.S Calcaneal Plating System of Biomet (K132898), • Gorilla® Plating System of Paragon28 (K190365), • ActivAnkle… | 2006 |
| * | K132898 | A.L.P.S. Calcaneal Plating SystemSummary page 5…t Medical Technology (K121651), • DARCO Locking Bone Plate System of Wright Medical Technology (K061808), • A.L.P.S Calcaneal Plating System of Biomet (K132898), • Gorilla® Plating System of Paragon28 (K190365), • ActivAnkle (K143061/K173641) of Newclip Technics. 4. Description of… | 2013 |
| * | K190365 | Baby Gorilla/Gorilla Plating SystemSummary page 5…ing Bone Plate System of Wright Medical Technology (K061808), • A.L.P.S Calcaneal Plating System of Biomet (K132898), • Gorilla® Plating System of Paragon28 (K190365), • ActivAnkle (K143061/K173641) of Newclip Technics. 4. Description of the device: The Footmotion Plating System consists… | 2019 |
| * | K143061 | Activ Ankle Locking Plating SystemSummary page 5…ight Medical Technology (K061808), • A.L.P.S Calcaneal Plating System of Biomet (K132898), • Gorilla® Plating System of Paragon28 (K190365), • ActivAnkle (K143061/K173641) of Newclip Technics. 4. Description of the device: The Footmotion Plating System consists of plates… | 2015 |
| * | K173641 | Activ AnkleSummary page 5…ical Technology (K061808), • A.L.P.S Calcaneal Plating System of Biomet (K132898), • Gorilla® Plating System of Paragon28 (K190365), • ActivAnkle (K143061/K173641) of Newclip Technics. 4. Description of the device: The Footmotion Plating System consists of plates… | 2018 |
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 26 years and passes through 6 companies; a new generation was cleared every 1.6 years on median.
- 38 of the 156 ancestors have a recall of any class.
- 3 other devices also cite its predicate K161448.
How does its category compare?
All HRS devicesHRS Plate, Fixation, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, 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 implants of the Footmotion Plating System are intended for arthrodeses, fractures and osteotomies fixation and revision surgeries of the foot in adults.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K221395 · printed Nov 5, 2026
Cite this page
510(k) Report. “K221395: Footmotion Plating System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K221395
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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