510(k) Report

510(k) · Cleared

Cleared

QUANTUM® Patient Specific Instrumentation (PSI) System

K211883510(k) TraditionalCleared Aug 11, 202151-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

In2bones Sas · HSN Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer

Cleared on Aug 11, 2021 as substantially equivalent to K162795 (Wrightmedicaltechnologyinc, 2017) and 1 other predicate after a 51-day review. Its family tree reaches back 9 generations to 1992. 2 later devices descend from it.

Decided
Aug 11, 2021
Review
51 days
Class
Class II
Product code
HSN
Recalls
None
Predicates
2

Its longest line of descent runs back 9 generations to K920802 (1992). 15 ancestors in all. 2 later devices descend from it, 2 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 deviceK211883 QUANTUM® Patient Specific Instrumentation (PSI) SystemIn2bones Sas · 2021
  7. Descendant · cites it directly · 0 of its ownK231699 QUANTUM® Patient Specific Instrumentation (PSI) SystemIn2bones Sas · 2024
  8. Descendant · cites it directly · 0 of its ownK230313 QUANTUM Patient Specific Instrumentation (PSI) SystemIn2bones Sas · 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 deviceK211883 QUANTUM® Patient Specific Instrumentation (PSI) SystemIn2bones Sas · 2021

Most influential descendants

Showing 2 of 2 · See all
  • K231699QUANTUM® Patient Specific Instrumentation (PSI) SystemIn2bones Sas · 2024 · cites it directly0descendants
  • K230313QUANTUM Patient Specific Instrumentation (PSI) SystemIn2bones Sas · 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)K211883QUANTUM® Patient Specific Instrumentation (PSI) SystemIn2bones Sas2021—
+1K231699QUANTUM® Patient Specific Instrumentation (PSI) SystemIn2bones Sas2024—
+1K230313QUANTUM Patient Specific Instrumentation (PSI) SystemIn2bones Sas2023—

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
202310
202410
FIG. 1 — Lineage of K211883, 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 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
Get a 510(k) 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.

TypeNumberDeviceApplicantDecidedRecalls
*K162795PROPHECY INVISION Preoperative Navigation Alignment System
Summary page 5
…proximal talus. Predicate Primary predicate: Devices PROPHECY INVISION Pre-operative Navigation System (K162795 & K170968), Wright Medical Technology Inc. Reference predicate: QUANTUM® Total Ankle Prosthe…
Wrightmedicaltechnologyinc2017—
*K170968PROPHECY INVISION Pre-operative Navigation System
Summary page 5
…roximal talus. Predicate Primary predicate: Devices PROPHECY INVISION Pre-operative Navigation System (K162795 & K170968), Wright Medical Technology Inc. Reference predicate: QUANTUM® Total Ankle Prosthesis (K1913…
Wrightmedicaltechnologyinc2017—
†K191380Quantum® Total Ankle ProsthesisIn2bones Sas2020—

Also cleared against K162795: 2 other devices →

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K231699QUANTUM® Patient Specific Instrumentation (PSI) SystemIn2bones Sas20240
K230313QUANTUM Patient Specific Instrumentation (PSI) SystemIn2bones Sas20230

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 29 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, K231699 (In2bones Sas, 2024) has gone furthest, with 0 descendants of its own.
  • 2 other devices also cite its predicate K162795.

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. 2021, 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?

In2Bones PSI: In2Bones QUANTUM® Patient Specific Instrumentation (PSI) Guides for Total Ankle Replacement (TAR) is indicated as an orthopaedic instrument system to assist in the instrumentation positioning dedicated to In2Bones QUANTUM® Total Ankle Replacement implantation. In2Bones QUANTUM® PSI guides are compatible with QUANTUMB® tibial tray, QUANTUM® tibial inlay, as well as standard and Flat-Cut QUANTUM® talar implants. PSI Guides are intended for…

Read the full statement (226 words)

In2Bones PSI: In2Bones QUANTUM® Patient Specific Instrumentation (PSI) Guides for Total Ankle Replacement (TAR) is indicated as an orthopaedic instrument system to assist in the instrumentation positioning dedicated to In2Bones QUANTUM® Total Ankle Replacement implantation. In2Bones QUANTUM® PSI guides are compatible with QUANTUMB® tibial tray, QUANTUM® tibial inlay, as well as standard and Flat-Cut QUANTUM® talar implants.

PSI Guides are intended for single use only. PSI Guides are manufactured in correlation with a pre-operative planning validated by the surgeon on the TAR Planning Software and assist in the positioning of the dedicated QUANTUM® instrumentation with which drillings or bone cuts will be performed. In2ZBones QUANTUM® PSI guides are indicated for patient population fulfilling the QUANTUM® Total Ankle Replacement indications and for which X-rays and CT-scan images are available and compliant with imaging protocol provided by In2Bones.

TAR Planning software: The TAR Planning Software is a preoperative surgical planning software intended to be used with In2Bones QUANTUM® Patient Specific Instrumentation (PSI) Guides and QUANTUM® Total Ankle Replacement. TAR Planning Software allows the surgeon to use advanced display and positioning tools to guide the marking of bone before cutting and preview the total ankle replacement components intraoperatively, provided that anatomic landmarks necessary for alignment and positioning of the implant are identifiable on patient X-rays and imaging scans. X-rays and CT-scan are the accepted imaging modalities for these procedures.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K211883: QUANTUM® Patient Specific Instrumentation (PSI) System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K211883

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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