510(k) · Cleared
ClearedTruemed Hand, Foot and Ankle Plates System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Truemed Group, LLC · HRS Plate, Fixation, Bone
Cleared on Jul 9, 2021 as substantially equivalent to K150099 (Synthes (USA) Products, LLC, 2015) and 8 other predicates after a 491-day review. Its family tree reaches back 13 generations to 1996.
- Decided
- Jul 9, 2021
- Review
- 491 days
- Class
- Class II
- Product code
- HRS
- Recalls
- None
- Predicates
- 9
Its longest line of descent runs back 13 generations to K962616 (1996). 109 ancestors in all, the oldest K792022 (1979). No later device cites it as a predicate yet.
- Root · 13 generations backK962616 Synthes Dorsal Distal Radius Plate (DDRP) SystemSynthes (Usa) · 1996
- 9 generations between
- 3 generations backK120070 Synthes Variable Angle LCP Elbow SystemSynthes USA · 2012 · Recalled
- 2 generations backK120717 Synthes Variable Angle LCP Elbow System (Medical and Posterolateral…Synthes USA · 2012
- 1 generation backK120854 Synthes VA LCP Ankle Trauma SystemSynthes USA · 2012
- This deviceK200575 Truemed Hand, Foot and Ankle Plates SystemTruemed Group, LLC · 2021
Show all 13 generations
- Root · 13 generations backK962616 Synthes Dorsal Distal Radius Plate (DDRP) SystemSynthes (Usa) · 1996
- 12 generations backK982732 Synthes (Usa) Distal Radius Plate System (DRPS)Synthes · 1998
- 11 generations backK023007 Distal Radius Fracture Repair SystemHand Innovations, Inc. · 2002
- 10 generations backK030198 Hand Innovations, Inc. Distal Radius Fracture Repair SystemHand Innovations, Inc. · 2003
- 9 generations backK032705 Distal Radius Fracture Repair SystemHand Innovations, Inc. · 2003
- 8 generations backK050932 Distal Volar Radius Anatomical Plate SystemHand Innovations, Inc. · 2005 · Recalled
- 7 generations backK051735 Peri-Loc Locking Bone Plates and Locking Bone Screws for the Upper…Smith & Nephew, Inc. · 2005
- 6 generations backK071563 Peri-Loc Periarticular Locked Plating SystemSmith & Nephew, Inc. · 2007
- 5 generations backK090675 Smith & Nephew, Inc. VLP Foot Plating, Screw System and AccessoriesSmith & Nephew, Inc. · 2009
- 4 generations backK100776 Synthes 2.4 MM/2.7 MM Variable Angle LCP Forefoot/Midfoot SystemSynthes (Usa) · 2010
- 3 generations backK120070 Synthes Variable Angle LCP Elbow SystemSynthes USA · 2012 · Recalled
- 2 generations backK120717 Synthes Variable Angle LCP Elbow System (Medical and Posterolateral…Synthes USA · 2012
- 1 generation backK120854 Synthes VA LCP Ankle Trauma SystemSynthes USA · 2012
- This deviceK200575 Truemed Hand, Foot and Ankle Plates SystemTruemed Group, LLC · 2021
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −13 | K962616 | Synthes Dorsal Distal Radius Plate (DDRP) System | Synthes (Usa) | 1996 | — |
| −12 | K982732 | Synthes (Usa) Distal Radius Plate System (DRPS) | Synthes | 1998 | — |
| −11 | K023007 | Distal Radius Fracture Repair System | Hand Innovations, Inc. | 2002 | — |
| −10 | K030198 | Hand Innovations, Inc. Distal Radius Fracture Repair System | Hand Innovations, Inc. | 2003 | — |
| −9 | K032705 | Distal Radius Fracture Repair System | Hand Innovations, Inc. | 2003 | — |
| −8 | K050932 | Distal Volar Radius Anatomical Plate System | Hand Innovations, Inc. | 2005 | 1 |
| −7 | K051735 | Peri-Loc Locking Bone Plates and Locking Bone Screws for the Upper Extremity | Smith & Nephew, Inc. | 2005 | — |
| −6 | K071563 | Peri-Loc Periarticular Locked Plating System | Smith & Nephew, Inc. | 2007 | — |
| −5 | K090675 | Smith & Nephew, Inc. VLP Foot Plating, Screw System and Accessories | Smith & Nephew, Inc. | 2009 | — |
| −4 | K100776 | Synthes 2.4 MM/2.7 MM Variable Angle LCP Forefoot/Midfoot System | Synthes (Usa) | 2010 | — |
| −3 | K120070 | Synthes Variable Angle LCP Elbow System | Synthes USA | 2012 | 1 |
| −2 | K120717 | Synthes Variable Angle LCP Elbow System (Medical and Posterolateral Distal… | Synthes USA | 2012 | — |
| −1 | K120854 | Synthes VA LCP Ankle Trauma System | Synthes USA | 2012 | — |
| 0 (this device) | K200575 | Truemed Hand, Foot and Ankle Plates System | Truemed Group, LLC | 2021 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1979 | 1 | 0 |
| 1989 | 1 | 0 |
| 1990 | 1 | 0 |
| 1991 | 1 | 0 |
| 1992 | 1 | 0 |
| 1993 | 2 | 0 |
| 1994 | 5 | 0 |
| 1995 | 2 | 0 |
| 1996 | 6 | 0 |
| 1997 | 1 | 0 |
| 1998 | 3 | 0 |
| 1999 | 3 | 0 |
| 2000 | 9 | 0 |
| 2001 | 10 | 0 |
| 2002 | 4 | 0 |
| 2003 | 5 | 0 |
| 2004 | 7 | 0 |
| 2005 | 6 | 0 |
| 2006 | 7 | 0 |
| 2007 | 3 | 0 |
| 2008 | 6 | 0 |
| 2009 | 3 | 0 |
| 2010 | 2 | 0 |
| 2011 | 3 | 0 |
| 2015 | 2 | 0 |
| 2017 | 1 | 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? (9)
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 |
|---|---|---|---|
| * | K150099 | Depuy Synthes Variable Angle Locking Hand System (1.3 mm and 2.0 mm Plates and Screws)Summary page 4…21 CFR 888.3030/21 CFR 888.3040 9. Regulation Numbers: PRIMARY PREDICATE 10. Predicate Devices: K150099 -Depuy Synthes Variable Angle Locking Hand System (1.3 Y 2.0 Mm Plates and Screws).… | 2015 |
| * | K030310 | Synthes Stainless Steel Modular Hand SystemSummary page 4…ocking Hand System (1.3 Y 2.0 Mm Plates and Screws). SECONDARY PREDICATES K030310 -Synthes Stainless Steel Modular Hand System. K050110-Synthes (USA) LCP Modular Foot Plates.… | 2003 |
| * | K050110 | Synthes (Usa) LCP Modular Foot PlatesSummary page 4…SECONDARY PREDICATES K030310 -Synthes Stainless Steel Modular Hand System. K050110-Synthes (USA) LCP Modular Foot Plates. K100776-Synthes 2.4 Mm / 2.7 Mm Variable Angle (Va)- LCP… | 2005 |
| * | K100776 | Synthes 2.4 MM/2.7 MM Variable Angle LCP Forefoot/Midfoot SystemSummary page 4…K030310 -Synthes Stainless Steel Modular Hand System. K050110-Synthes (USA) LCP Modular Foot Plates. K100776-Synthes 2.4 Mm / 2.7 Mm Variable Angle (Va)- LCP Forefoot/Midfoot System.… | 2010 |
| * | K071264 | Synthes (Usa) 2.4/2.7 MM Locking Foot ModuleSummary page 4…K100776-Synthes 2.4 Mm / 2.7 Mm Variable Angle (Va)- LCP Forefoot/Midfoot System. K071264-Synthes (USA) 2.4/2.7mm Locking Foot Module. K020401-Synthes Calcaneal Plate.… | 2007 |
| * | K020401 | Synthes Calcaneal PlateSummary page 4…Forefoot/Midfoot System. K071264-Synthes (USA) 2.4/2.7mm Locking Foot Module. K020401-Synthes Calcaneal Plate. K120854-Synthes Variable Angle LCP Ankle Trauma System.… | 2002 |
| * | K120854 | Synthes VA LCP Ankle Trauma SystemSummary page 4…K071264-Synthes (USA) 2.4/2.7mm Locking Foot Module. K020401-Synthes Calcaneal Plate. K120854-Synthes Variable Angle LCP Ankle Trauma System. K143191-McGinley Innovations IntelliSense Drill.… | 2012 |
| * | K143191 | IntelliSense DrillSummary page 4…K020401-Synthes Calcaneal Plate. K120854-Synthes Variable Angle LCP Ankle Trauma System. K143191-McGinley Innovations IntelliSense Drill. K182650- Arzzt Distal Radius And Ulna System. === Page… | 2015 |
| * | K182650 | Arzzt Distal Radius and Ulna SystemSummary page 4…K120854-Synthes Variable Angle LCP Ankle Trauma System. K143191-McGinley Innovations IntelliSense Drill. K182650- Arzzt Distal Radius And Ulna System.… | 2019 |
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 25 years and passes through 6 companies; a new generation was cleared every 1.6 years on median.
- 26 of the 109 ancestors have a recall of any class.
- 5 other devices also cite its predicate K150099.
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?
Intended use for fixation of complex intra and extra-articular fractures and osteotomies, selective trauma, reconstructive procedures, fusions osteotomies, non-unions, replantations, complex extra articular fractures and fusions of bones of the anatomical regions of the hand, foot and ankle, particularly for osteopenic bone in adults and adolescents.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K200575 · printed Nov 6, 2026
Cite this page
510(k) Report. “K200575: Truemed Hand, Foot and Ankle Plates System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K200575
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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