510(k) · Cleared
ClearedCadence Ankle PSI System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
3D Systems, Inc. · OYK Ankle Arthroplasty Implantation System
Cleared on Oct 25, 2024 as substantially equivalent to K241326 (3D Systems, Inc., 2024) after a 25-day review. Its family tree reaches back 11 generations to 1992.
- Decided
- Oct 25, 2024
- Review
- 25 days
- Class
- Class II
- Product code
- OYK
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 11 generations to K920802 (1992). 17 ancestors in all. No later device cites it as a predicate yet.
- Root · 11 generations backK920802 Alvine Total AnkleDepuy, Inc. · 1992
- 7 generations between
- 3 generations backK170968 PROPHECY INVISION Pre-operative Navigation SystemWrightmedicaltechnologyinc · 2017
- 2 generations backK193432 Vantage PSI System3D Systems · 2020
- 1 generation backK241326 Cadence Ankle PSI System3D Systems, Inc. · 2024
- This deviceK243174 Cadence Ankle PSI System3D Systems, Inc. · 2024
Show all 11 generations
- Root · 11 generations backK920802 Alvine Total AnkleDepuy, Inc. · 1992
- 10 generations backK020541 Agility Ankle Revision ProsthesisDepuy, Inc. · 2002
- 9 generations backK051023 Topez Total Ankle ReplacementTopez Orthopedics, Inc. · 2005 · Recalled
- 8 generations backK100886 Inbone II Total Ankle ReplacementWrightmedicaltechnologyinc · 2010 · Recalled
- 7 generations backK123954 Infinity Total Ankle SystemWrightmedicaltechnologyinc · 2013 · Recalled
- 6 generations backK133585 Inbone Total AnkleWrightmedicaltechnologyinc · 2014
- 5 generations backK142117 Invision Total Ankle Revision SystemWrightmedicaltechnologyinc · 2015
- 4 generations backK162795 PROPHECY INVISION Preoperative Navigation Alignment SystemWrightmedicaltechnologyinc · 2017
- 3 generations backK170968 PROPHECY INVISION Pre-operative Navigation SystemWrightmedicaltechnologyinc · 2017
- 2 generations backK193432 Vantage PSI System3D Systems · 2020
- 1 generation backK241326 Cadence Ankle PSI System3D Systems, Inc. · 2024
- This deviceK243174 Cadence Ankle PSI System3D Systems, Inc. · 2024
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −11 | K920802 | Alvine Total Ankle | Depuy, Inc. | 1992 | — |
| −10 | K020541 | Agility Ankle Revision Prosthesis | Depuy, Inc. | 2002 | — |
| −9 | K051023 | Topez Total Ankle Replacement | Topez Orthopedics, Inc. | 2005 | 4 |
| −8 | K100886 | Inbone II Total Ankle Replacement | Wrightmedicaltechnologyinc | 2010 | 2 |
| −7 | K123954 | Infinity Total Ankle System | Wrightmedicaltechnologyinc | 2013 | 2 |
| −6 | K133585 | Inbone Total Ankle | Wrightmedicaltechnologyinc | 2014 | — |
| −5 | K142117 | Invision Total Ankle Revision System | Wrightmedicaltechnologyinc | 2015 | — |
| −4 | K162795 | PROPHECY INVISION Preoperative Navigation Alignment System | Wrightmedicaltechnologyinc | 2017 | — |
| −3 | K170968 | PROPHECY INVISION Pre-operative Navigation System | Wrightmedicaltechnologyinc | 2017 | — |
| −2 | K193432 | Vantage PSI System | 3D Systems | 2020 | — |
| −1 | K241326 | Cadence Ankle PSI System | 3D Systems, Inc. | 2024 | — |
| 0 (this device) | K243174 | Cadence Ankle PSI System | 3D Systems, Inc. | 2024 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2006 | 1 | 0 |
| 2010 | 1 | 0 |
| 2011 | 1 | 0 |
| 2013 | 1 | 0 |
| 2014 | 1 | 0 |
| 2016 | 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 OYK? 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 OYK device
- #1 K193432 Vantage PSI Systemscore 14.7 · 9 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (1)
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 |
|---|---|---|---|
| * | K241326 | Cadence Ankle PSI SystemSummary page 5…al/polymer semi-constrained cemented prosthesis Classification: Class II, 21 CFR 888.3110 Product Code: OYK 4. PREDICATE DEVICE Predicate Device: K241326 Cadence Ankle PSI System, Product Code OYK 5. REFERENCE DEVICE Reference Device: K201507 Cadence Total Ankle System, Produc… | 2024 |
| † | K201507 | Cadence Total Ankle System | 2020 |
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 32 years and passes through 5 companies; a new generation was cleared every 2.6 years on median.
- 4 of the 17 ancestors have a recall of any class.
How does its category compare?
All OYK devicesOYK Ankle Arthroplasty Implantation System: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.
FDA decisions per year · OYK
4in 2024
2026 to Oct 25, outlined.
Median 510(k) review, days · OYK
69in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · OYK
1in 2011
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · OYK
2in 2025
MAUDE reports naming product code OYK, 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 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 1 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 1 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 4 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 2 | — | 0 | 1 |
| 2024 | 4 | 69 | 0 | 2 |
| 2025 | 0 | — | 0 | 2 |
| 2026 | 0 | — | 1 | — |
What is it indicated for?
The Cadence Ankle PSI System is intended to be used as patient specific surgical planning and
instrumentation to assist in the positioning of total ankle replacement components intraoperatively,
and in guiding bone cutting. The Cadence Ankle PSI System is intended for use with Smith +
Nephew's Cadence Total Ankle System and its cleared indications for use, provided that anatomic
landmarks necessary for alignment and positioning of the implant are identifiable on patient imaging
CT scans.
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/K243174 · printed Nov 6, 2026
Cite this page
510(k) Report. “K243174: Cadence Ankle PSI System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K243174
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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