510(k) Report

510(k) · Cleared

Cleared

Vantage PSI System

K193432510(k) TraditionalCleared Nov 9, 2020335-day reviewClass II21 CFR 888.3110

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

3D Systems · OYK Ankle Arthroplasty Implantation System

Cleared on Nov 9, 2020 as substantially equivalent to K170968 (Wrightmedicaltechnologyinc, 2017) after a 335-day review. Its family tree reaches back 9 generations to 1992. 6 later devices descend from it.

Decided
Nov 9, 2020
Review
335 days
Class
Class II
Product code
OYK
Recalls
None
Predicates
1

Its longest line of descent runs back 9 generations to K920802 (1992). 15 ancestors in all. 6 later devices descend from it, 4 citing it directly.

  1. Root · 9 generations backK920802 Alvine Total AnkleDepuy, Inc. · 1992
  2. 5 generations between
  3. 3 generations backK142117 Invision Total Ankle Revision SystemWrightmedicaltechnologyinc · 2015
  4. 2 generations backK162795 PROPHECY INVISION Preoperative Navigation Alignment SystemWrightmedicaltechnologyinc · 2017
  5. 1 generation backK170968 PROPHECY INVISION Pre-operative Navigation SystemWrightmedicaltechnologyinc · 2017
  6. This deviceK193432 Vantage PSI System3D Systems · 2020
  7. Descendant · cites it directly · 1 of its ownK241326 Cadence Ankle PSI System3D Systems, Inc. · 2024
  8. Descendant · cites it directly · 1 of its ownK241148 Salto Talaris Ankle PSI System3D Systems, Inc. · 2024
  9. Descendant · 2 generations on · 0 of its ownK243173 Salto Talaris Ankle PSI System3D Systems, Inc. · 2024
  10. Descendant · 2 generations on · 0 of its ownK243174 Cadence Ankle PSI System3D Systems, Inc. · 2024
  11. Descendant · cites it directly · 0 of its ownK231585 Vantage PSI System3D Systems, Inc. · 2023
Show all 9 generations
  1. Root · 9 generations backK920802 Alvine Total AnkleDepuy, Inc. · 1992
  2. 8 generations backK020541 Agility Ankle Revision ProsthesisDepuy, Inc. · 2002
  3. 7 generations backK051023 Topez Total Ankle ReplacementTopez Orthopedics, Inc. · 2005 · Recalled
  4. 6 generations backK100886 Inbone II Total Ankle ReplacementWrightmedicaltechnologyinc · 2010 · Recalled
  5. 5 generations backK123954 Infinity Total Ankle SystemWrightmedicaltechnologyinc · 2013 · Recalled
  6. 4 generations backK133585 Inbone Total AnkleWrightmedicaltechnologyinc · 2014
  7. 3 generations backK142117 Invision Total Ankle Revision SystemWrightmedicaltechnologyinc · 2015
  8. 2 generations backK162795 PROPHECY INVISION Preoperative Navigation Alignment SystemWrightmedicaltechnologyinc · 2017
  9. 1 generation backK170968 PROPHECY INVISION Pre-operative Navigation SystemWrightmedicaltechnologyinc · 2017
  10. This deviceK193432 Vantage PSI System3D Systems · 2020

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

2023: 22024: 4
2023high 4 (2024) · low 0 (2025)2026

Most influential descendants

Showing 5 of 6 · See all
  • K241326Cadence Ankle PSI System3D Systems, Inc. · 2024 · cites it directly1descendant
  • K241148Salto Talaris Ankle PSI System3D Systems, Inc. · 2024 · cites it directly1descendant
  • K243173Salto Talaris Ankle PSI System3D Systems, Inc. · 2024 · 2 generations on0descendants
  • K243174Cadence Ankle PSI System3D Systems, Inc. · 2024 · 2 generations on0descendants
  • K231585Vantage PSI System3D Systems, Inc. · 2023 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K920802Alvine Total AnkleDepuy, Inc.1992—
−8K020541Agility Ankle Revision ProsthesisDepuy, Inc.2002—
−7K051023Topez Total Ankle ReplacementTopez Orthopedics, Inc.20054
−6K100886Inbone II Total Ankle ReplacementWrightmedicaltechnologyinc20102
−5K123954Infinity Total Ankle SystemWrightmedicaltechnologyinc20132
−4K133585Inbone Total AnkleWrightmedicaltechnologyinc2014—
−3K142117Invision Total Ankle Revision SystemWrightmedicaltechnologyinc2015—
−2K162795PROPHECY INVISION Preoperative Navigation Alignment SystemWrightmedicaltechnologyinc2017—
−1K170968PROPHECY INVISION Pre-operative Navigation SystemWrightmedicaltechnologyinc2017—
0 (this device)K193432Vantage PSI System3D Systems2020—
+1K241326Cadence Ankle PSI System3D Systems, Inc.2024—
+1K241148Salto Talaris Ankle PSI System3D Systems, Inc.2024—
+2K243173Salto Talaris Ankle PSI System3D Systems, Inc.2024—
+2K243174Cadence Ankle PSI System3D Systems, Inc.2024—
+1K231585Vantage PSI System3D Systems, Inc.2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200610
201010
201110
201310
201410
201610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202320
202440
FIG. 1 — Lineage of K193432, 1992–2024Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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. #1 K241326 Cadence Ankle PSI Systemscore 13.6 · 10 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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.

TypeNumberDeviceApplicantDecidedRecalls
*K170968PROPHECY INVISION Pre-operative Navigation System
Summary page 4
…Code: OYK 4. PREDICATE DEVICES Predicate device: • PROPHECY® INVISION® Preoperative Navigation Alignment Guides, Wright Medical Technology, Inc.(K170968) Reference devices: • VSP® Orthopedics System, 3D Systems Inc. (K190044) 5. DESCRIPTION OF THE DEVICE 3D System’s Vant…
Wrightmedicaltechnologyinc2017—
†K190044VSP Orthopedics System3D Systems, Inc.2019—

Also cleared against K170968: 3 other devices →

What descends from it? (6)

4 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K241326Cadence Ankle PSI System3D Systems, Inc.20241
K241148Salto Talaris Ankle PSI System3D Systems, Inc.20241
K231585Vantage PSI System3D Systems, Inc.20230
K223326Axiom PSR SystemRestor3D20230

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 28 years and passes through 4 companies; a new generation was cleared every 2.6 years on median.
  • 4 of the 15 ancestors have a recall of any class.
  • Of its descendants, K241326 (3D Systems, Inc., 2024) has gone furthest, with 1 descendant of its own.
  • 3 other devices also cite its predicate K170968.

How does its category compare?

All OYK devices

OYK Ankle Arthroplasty Implantation System: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · OYK

4in 2024

2020: 12023: 22024: 4
2007high 4 (2024) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OYK

69in 2024

2024: 69 days median
2007high 69 (2024)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · OYK

1in 2011

2011: 12026 (partial year): 1
2007high 1 (2011) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · OYK

2in 2025

2021: 42023: 12024: 22025: 2
2007high 4 (2021) · low 0 (2007)2025

MAUDE reports naming product code OYK, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—10
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20201—00
20210—04
20220—00
20232—01
202446902
20250—02
20260—1—

What is it indicated for?

The Vantage 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 Vantage PSI System is intended for use with Exactech’s Vantage Total Ankle System and its cleared indications for use.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K193432: Vantage 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/K193432

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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