510(k) Report

510(k) · Cleared

Cleared

INVISION Total Ankle Revision System

K180730510(k) TraditionalCleared Jul 11, 2018113-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

Wrightmedicaltechnologyinc · HSN Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer

Cleared on Jul 11, 2018 as substantially equivalent to K171067 (Wrightmedicaltechnologyinc, 2017) and 3 other predicates after a 113-day review. Its family tree reaches back 8 generations to 1992. 3 later devices descend from it.

Decided
Jul 11, 2018
Review
113 days
Class
Class II
Product code
HSN
Recalls
None
Predicates
4

Its longest line of descent runs back 8 generations to K920802 (1992). 14 ancestors in all. 3 later devices descend from it, 1 citing it directly.

  1. Root · 8 generations backK920802 Alvine Total AnkleDepuy, Inc. · 1992
  2. 7 generations backK020541 Agility Ankle Revision ProsthesisDepuy, Inc. · 2002
  3. 6 generations backK051023 Topez Total Ankle ReplacementTopez Orthopedics, Inc. · 2005 · Recalled
  4. 5 generations backK100886 Inbone II Total Ankle ReplacementWrightmedicaltechnologyinc · 2010 · Recalled
  5. 4 generations backK123954 Infinity Total Ankle SystemWrightmedicaltechnologyinc · 2013 · Recalled
  6. 3 generations backK140749 Infinity Total Ankle SystemWrightmedicaltechnologyinc · 2014 · Recalled
  7. 2 generations backK141740 Infinity (TM) Total Ankle System; Inbone Total Ankle SystemWrightmedicaltechnologyinc · 2015
  8. 1 generation backK171067 INVISION Total Ankle Revision SystemWrightmedicaltechnologyinc · 2017
  9. This deviceK180730 INVISION Total Ankle Revision SystemWrightmedicaltechnologyinc · 2018
  10. Descendant · cites it directly · 2 of its ownK193067 The INBONE™ Total Ankle System, the INFINITY™ Total Ankle System and…Wrightmedicaltechnologyinc · 2020
  11. Descendant · 2 generations on · 1 of its ownK250037 Incompass Total Ankle SystemWright Medical Technology, Inc. (Stryker) · 2025
  12. Descendant · 3 generations on · 0 of its ownK253159 Prophecy Incompass Surgical Planning SystemWright Medical Technology, Inc. (Stryker) · 2026

Most influential descendants

Showing 3 of 3 · See all
  • K193067The INBONE™ Total Ankle System, the INFINITY™ Total Ankle System and the INVISION™ Total…Wrightmedicaltechnologyinc · 2020 · cites it directly2descendants
  • K250037Incompass Total Ankle SystemWright Medical Technology, Inc. (Stryker) · 2025 · 2 generations on1descendant
  • K253159Prophecy Incompass Surgical Planning SystemWright Medical Technology, Inc. (Stryker) · 2026 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K920802Alvine Total AnkleDepuy, Inc.1992—
−7K020541Agility Ankle Revision ProsthesisDepuy, Inc.2002—
−6K051023Topez Total Ankle ReplacementTopez Orthopedics, Inc.20054
−5K100886Inbone II Total Ankle ReplacementWrightmedicaltechnologyinc20102
−4K123954Infinity Total Ankle SystemWrightmedicaltechnologyinc20132
−3K140749Infinity Total Ankle SystemWrightmedicaltechnologyinc20141
−2K141740Infinity (TM) Total Ankle System; Inbone Total Ankle SystemWrightmedicaltechnologyinc2015—
−1K171067INVISION Total Ankle Revision SystemWrightmedicaltechnologyinc2017—
0 (this device)K180730INVISION Total Ankle Revision SystemWrightmedicaltechnologyinc2018—
+1K193067The INBONE™ Total Ankle System, the INFINITY™ Total Ankle System and the…Wrightmedicaltechnologyinc2020—
+2K250037Incompass Total Ankle SystemWright Medical Technology, Inc. (Stryker)2025—
+3K253159Prophecy Incompass Surgical Planning SystemWright Medical Technology, Inc. (Stryker)2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200610
201010
201310
201410
201510
201610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
202510
202610
FIG. 1 — Lineage of K180730, 1992–2026Source: 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 HSN? 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 HSN device

  1. #1 K192994 Paragon 28 APEX 3D Total Ankle Replacement…score 16.8 · 8 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? (4)

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
*K171067INVISION Total Ankle Revision System
Summary page 4
…de & Panel: HSN – Orthopedic (a)(3) PREDICATE DEVICE INFORMATION INVISION Total Ankle Revision System – Primary Predicate K171067 INVISION Total Ankle Revision System K153008 INBONE Total Ankle System…
Wrightmedicaltechnologyinc2017—
*K153008INVISION Total Ankle Revision System
Summary page 4
…TION INVISION Total Ankle Revision System – Primary Predicate K171067 INVISION Total Ankle Revision System K153008 INBONE Total Ankle System K103374, K133585 (a)(4) DEVICE DESCRIPTON…
Wrightmedicaltechnologyinc2016—
*K103374Inbone Total Ankle System Model 200347902
Summary page 4
…71067 INVISION Total Ankle Revision System K153008 INBONE Total Ankle System K103374, K133585 (a)(4) DEVICE DESCRIPTON The INVISION Total Ankle Revision System is a fixed-bearing ankle replacement…
Wrightmedicaltechnologyinc2010—
*K133585Inbone Total Ankle
Summary page 4
…INVISION Total Ankle Revision System K153008 INBONE Total Ankle System K103374, K133585 (a)(4) DEVICE DESCRIPTON The INVISION Total Ankle Revision System is a fixed-bearing ankle replacement prosthes…
Wrightmedicaltechnologyinc2014—

Also cleared against K171067: 1 other device →

What descends from it? (3)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K193067The INBONE™ Total Ankle System, the INFINITY™ Total Ankle System and the INVISION™ Total…Wrightmedicaltechnologyinc20202

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 3 companies; a new generation was cleared every 2.6 years on median.
  • 4 of the 14 ancestors have a recall of any class.
  • Of its descendants, K193067 (Wrightmedicaltechnologyinc, 2020) has gone furthest, with 2 descendants of its own.
  • 1 other device also cites its predicate K171067.

How does its category compare?

All HSN devices

HSN Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.

FDA decisions per year · HSN

3in 2025

2009: 12010: 22011: 12012: 22013: 42014: 22015: 32016: 32017: 42018: 42019: 22020: 62021: 42022: 12023: 62024: 72025: 32026 (partial year): 2
2007high 7 (2024) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HSN

58in 2025

2013: 89 days median2015: 233 days median2016: 216 days median2017: 148 days median2018: 89 days median2020: 234 days median2021: 109 days median2023: 112 days median2024: 115 days median2025: 58 days median
2007high 234 (2020) · low 58 (2025)2026

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

Recalls per year · HSN

1in 2023

2013: 32016: 12017: 22019: 12021: 32022: 22023: 1
2007high 3 (2013) · low 0 (2007)2026

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

Adverse event reports per year · HSN

1,645in 2025

2007: 502008: 662009: 662010: 1202011: 1392012: 1002013: 1062014: 652015: 732016: 1112017: 962018: 1872019: 2772020: 2812021: 2372022: 4532023: 7962024: 1,0952025: 1,645
2007high 1,645 (2025) · low 50 (2007)2025

MAUDE reports naming product code HSN, 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—050
20080—066
20091—066
20102—0120
20111—0139
20122—0100
20134893106
20142—065
20153233073
201632161111
20174148296
20184890187
20192—1277
202062340281
202141093237
20221—2453
202361121796
2024711501,095
202535801,645
20262—0—

What is it indicated for?

The INVISION™ Total Ankle Revision System is indicated for patients with ankle joints damaged by severe rheumatoid, post-traumatic, or degenerative arthritis.

The INVISION™ Total Ankle Revision System is additionally indicated for patients with a failed previous ankle surgery.

CAUTION: In the United States, the ankle prosthesis is intended for cement use only.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K180730: INVISION Total Ankle Revision System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K180730

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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