510(k) Report

510(k) · Cleared

Cleared

Rotaglide + Modular Knee System with Fixed Meniscus

K000232510(k) SpecialCleared Feb 25, 200029-day reviewClass II21 CFR 888.3560

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

Corin USA · JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Cleared on Feb 25, 2000 after a 29-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 4 later devices descend from it.

Decided
Feb 25, 2000
Review
29 days
Class
Class II
Product code
JWH
Recalls
None
Predicates
0

4 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2002: 1 descendant cleared2011: 1 descendant cleared2003: 1 descendant cleared2012: 1 descendant cleared200020052010201520202025
  1. This deviceK000232 Rotaglide + Modular Knee System with Fixed MeniscusCorin USA · 2000
  2. Descendant · cites it directly · 3 of its ownK013906 HLS Noetos SystemTornier · 2002
  3. Descendant · 2 generations on · 1 of its ownK094013 HLS Kneetec SystemTornier · 2011
  4. Descendant · 3 generations on · 0 of its ownK111970 Kneetec PFJ&HLS Kneetec Patellar ComponentTornier · 2012
  5. Descendant · 2 generations on · 0 of its ownK032079 HLS Noetos SystemTornier · 2003

Most influential descendants

Showing 4 of 4 · See all
  • K013906HLS Noetos SystemTornier · 2002 · cites it directly3descendants
  • K094013HLS Kneetec SystemTornier · 2011 · 2 generations on1descendant
  • K111970Kneetec PFJ&HLS Kneetec Patellar ComponentTornier · 2012 · 3 generations on0descendants
  • K032079HLS Noetos SystemTornier · 2003 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K000232Rotaglide + Modular Knee System with Fixed MeniscusCorin USA2000—
+1K013906HLS Noetos SystemTornier2002—
+2K094013HLS Kneetec SystemTornier2011—
+3K111970Kneetec PFJ&HLS Kneetec Patellar ComponentTornier2012—
+2K032079HLS Noetos SystemTornier2003—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200210
200310
201110
201210
FIG. 1 — Lineage of K000232, 2000–2012Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in JWH? 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 JWH device

  1. #1 K221479 Persona Personalized Knee Systemscore 22.4 · 11 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?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (4)

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

NumberDeviceApplicantDecidedDescendants
K013906HLS Noetos SystemTornier20023

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?

  • Of its descendants, K013906 (Tornier, 2002) has gone furthest, with 3 descendants of its own.

How does its category compare?

All JWH devices

JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · JWH

20in 2025

2007: 182008: 172009: 112010: 192011: 252012: 332013: 312014: 332015: 272016: 182017: 252018: 252019: 282020: 222021: 242022: 172023: 202024: 192025: 202026 (partial year): 12
2007high 33 (2012) · low 11 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JWH

55in 2025

2007: 74 days median2008: 81 days median2009: 168 days median2010: 85 days median2011: 87 days median2012: 85 days median2013: 128 days median2014: 98 days median2015: 87 days median2016: 88 days median2017: 118 days median2018: 90 days median2019: 133 days median2020: 59 days median2021: 61 days median2022: 56 days median2023: 57 days median2024: 89 days median2025: 55 days median2026 (partial year): 63 days median
2007high 168 (2009) · low 55 (2025)2026

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

Recalls per year · JWH

2in 2025

2007: 142008: 102009: 1092010: 322011: 272012: 852013: 312014: 132015: 112016: 172017: 612018: 142019: 52020: 22021: 82022: 122023: 672024: 72025: 22026 (partial year): 4
2007high 109 (2009) · low 2 (2020)2026

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

Adverse event reports per year · JWH

9,306in 2025

2007: 1,3052008: 1,4832009: 1,8702010: 3,2862011: 5,1332012: 5,2032013: 6,1352014: 6,7222015: 6,8812016: 7,5862017: 12,2632018: 14,0712019: 14,9872020: 12,5922021: 9,4082022: 8,3642023: 8,9472024: 10,8282025: 9,306
2007high 14,987 (2019) · low 1,305 (2007)2025

MAUDE reports naming product code JWH, 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
20071874141,305
20081781101,483
2009111681091,870
20101985323,286
20112587275,133
20123385855,203
201331128316,135
20143398136,722
20152787116,881
20161888177,586
2017251186112,263
201825901414,071
201928133514,987
20202259212,592
2021246189,408
20221756128,364
20232057678,947
20241989710,828
2025205529,306
202612634—

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https://510kreport.com/device/K000232 · printed Nov 6, 2026

Cite this page

510(k) Report. “K000232: Rotaglide + Modular Knee System with Fixed Meniscus.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K000232

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026