510(k) · Cleared
ClearedWRISTAR MultiAx Distal Radius Kit
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Intrauma S.P.A · HRS Plate, Fixation, Bone
Cleared on Nov 12, 2025 as substantially equivalent to K083694 (Synthes (Usa), 2009) and 1 other predicate after a 57-day review. Its family tree reaches back 1 generation to 2007.
- Decided
- Nov 12, 2025
- Review
- 57 days
- Class
- Class II
- Product code
- HRS
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 1 generation to K071184 (2007). 2 ancestors in all. No later device cites it as a predicate yet.
- Root · 1 generation backK071184 Synthes (Usa) Variable Angle-Locking Compression Plate (VA-LCP)…Synthes (Usa) · 2007 · Recalled
- This deviceK252959 WRISTAR MultiAx Distal Radius KitIntrauma S.P.A · 2025
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K071184 | Synthes (Usa) Variable Angle-Locking Compression Plate (VA-LCP) Distal Radius… | Synthes (Usa) | 2007 | 1 |
| 0 (this device) | K252959 | WRISTAR MultiAx Distal Radius Kit | Intrauma S.P.A | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2009 | 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? (2)
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 |
|---|---|---|---|
| * | K083694 | Synthes (Usa) 2.4 MM VA-LCP Two Column Volar Distal Radius PlatesSummary page 5…HWC - Screw, Fixation, Bone Synthes 2.4mm VA-LCP Two-Column Volar Distal Radius Primary Predicate: Plate (K083694) Synthes 2.4mm Variable Angle-Locking Compression Plate Additional Predicate: (VA-LCP) Dis… | 2009 |
| * | K071184 | Synthes (Usa) Variable Angle-Locking Compression Plate (VA-LCP) Distal Radius SystemSummary page 5…Plate (K083694) Synthes 2.4mm Variable Angle-Locking Compression Plate Additional Predicate: (VA-LCP) Distal Radius System (K071184) Indications For Use: The Wristar MultiAx Distal Radius Kit is indicated for: - Fixation of complex intra- and extra-articular… | 2007 |
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?
- 2 of the 2 ancestors have a recall of any class.
- 11 other devices also cite its predicate K083694.
How does its category compare?
All HRS devicesHRS Plate, Fixation, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, 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 Wristar MultiAx Distal Radius Kit is indicated for:
- Fixation of complex intra- and extra-articular fractures of the distal radius
- osteotomies of the distal radius
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K252959 · printed Nov 4, 2026
Cite this page
510(k) Report. “K252959: WRISTAR MultiAx Distal Radius Kit.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K252959
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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