510(k) Report

510(k) · Cleared

Cleared

Total Knee Surgetics Navigation System

K060282510(k) SpecialCleared Apr 10, 200666-day reviewClass II21 CFR 882.4560

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

Praxim S.A · HAW Neurological Stereotaxic Instrument

Cleared on Apr 10, 2006 as substantially equivalent to K031196 (Praxim, 2005) after a 66-day review. Its family tree reaches back 3 generations to 2000. 147 later devices descend from it.

Decided
Apr 10, 2006
Review
66 days
Class
Class II
Product code
HAW
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K002053 (2000). 6 ancestors in all. 147 later devices descend from it, 6 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2002: 1 other ancestor2001: 2 other ancestors2006: 1 descendant cleared2007: 3 descendants cleared2009: 3 descendants cleared2008: 3 descendants cleared2010: 4 descendants cleared2011: 1 descendant cleared2016: 5 descendants cleared2017: 15 descendants cleared2012: 4 descendants cleared2021: 7 descendants cleared2013: 2 descendants cleared2019: 7 descendants cleared2020: 13 descendants cleared2014: 4 descendants cleared2025: 16 descendants cleared2026: 11 descendants cleared2023: 16 descendants cleared2022: 12 descendants cleared2024: 14 descendants cleared2015: 5 descendants cleared2018: 1 descendant clearedK002053 · Navitrak System-Optical Option, Model 900.004 · Orthosoft, Inc. · 2000K021760 · Navitrack System-Optical TKR CT-Less, Model 900.120 · Orthosoft, Inc. · 2002K031196 · Surgetics Ortho Kneelogics Navigation System · Praxim · 2005200020052010201520202025
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor3 generations back: 2 other ancestors 1 generation forward: 6 descendants2 generations forward: 6 descendants3 generations forward: 11 descendants4 generations forward: 16 descendants5 generations forward: 18 descendants6 generations forward: 18 descendants7 generations forward: 13 descendants8 generations forward: 11 descendants9 generations forward: 14 descendants10 generations forward: 15 descendants11 generations forward: 6 descendants12 generations forward: 4 descendants13 generations forward: 2 descendants14 generations forward: 2 descendants15 generations forward: 1 descendant16 generations forward: 1 descendant17 generations forward: 1 descendant18 generations forward: 1 descendant19 generations forward: 1 descendant K031196 · Surgetics Ortho Kneelogics Navigation System · Praxim · 2005K021760 · Navitrack System-Optical TKR CT-Less, Model 900.120 · Orthosoft, Inc. · 2002K002053 · Navitrak System-Optical Option, Model 900.004 · Orthosoft, Inc. · 20000+5+10+15
  1. Root · 3 generations backK002053 Navitrak System-Optical Option, Model 900.004Orthosoft, Inc. · 2000
  2. 2 generations backK021760 Navitrack System-Optical TKR CT-Less, Model 900.120Orthosoft, Inc. · 2002
  3. 1 generation backK031196 Surgetics Ortho Kneelogics Navigation SystemPraxim · 2005
  4. This deviceK060282 Total Knee Surgetics Navigation SystemPraxim S.A · 2006
  5. Descendant · cites it directly · 99 of its ownK062146 Uni Knee Surgetics Navigation SystemPraxim S.A · 2006
  6. Descendant · 2 generations on · 79 of its ownK071714 Navitrack System - OS Unicondylar Knee Universal, Model# Pro-06003Orthosoft, Inc. · 2007 · Recalled
  7. Descendant · 2 generations on · 78 of its ownK072806 Mako Surgical Tactile Guidance System (TGS)Mako Surgical Corp. · 2008 · Recalled
  8. Descendant · 3 generations on · 76 of its ownK081867 Mako Surgical Tactile Guidance System Version 2.0Mako Surgical Corp. · 2008 · Recalled
  9. Descendant · 4 generations on · 46 of its ownK112507 Restoris Partial Knee Application (Pka), Rio Standard SystemMako Surgical Corporation · 2012 · Recalled

Showing 5 of 147 descendants. See all descendants

Descendants cleared per year

2006: 12007: 32008: 32009: 32010: 42011: 12012: 42013: 22014: 42015: 52016: 52017: 152018: 12019: 72020: 132021: 72022: 122023: 162024: 142025: 162026: 11
2006high 16 (2023) · low 1 (2006)2026

Most influential descendants

Showing 5 of 147 · See all
  • K062146Uni Knee Surgetics Navigation SystemPraxim S.A · 2006 · cites it directly99descendants
  • K071714Navitrack System - OS Unicondylar Knee Universal, Model# Pro-06003Orthosoft, Inc. · 2007 · 2 generations on79descendants
  • K072806Mako Surgical Tactile Guidance System (TGS)Mako Surgical Corp. · 2008 · 2 generations on78descendants
  • K081867Mako Surgical Tactile Guidance System Version 2.0Mako Surgical Corp. · 2008 · 3 generations on76descendants
  • K112507Restoris Partial Knee Application (Pka), Rio Standard SystemMako Surgical Corporation · 2012 · 4 generations on46descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K002053Navitrak System-Optical Option, Model 900.004Orthosoft, Inc.2000—
−2K021760Navitrack System-Optical TKR CT-Less, Model 900.120Orthosoft, Inc.2002—
−1K031196Surgetics Ortho Kneelogics Navigation SystemPraxim2005—
0 (this device)K060282Total Knee Surgetics Navigation SystemPraxim S.A2006—
+1K062146Uni Knee Surgetics Navigation SystemPraxim S.A2006—
+2K071714Navitrack System - OS Unicondylar Knee Universal, Model# Pro-06003Orthosoft, Inc.20072
+2K072806Mako Surgical Tactile Guidance System (TGS)Mako Surgical Corp.20081
+3K081867Mako Surgical Tactile Guidance System Version 2.0Mako Surgical Corp.20082
+4K112507Restoris Partial Knee Application (Pka), Rio Standard SystemMako Surgical Corporation20126

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200120
200210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200610
200730
200830
200930
201040
201110
201240
201320
201440
201550
201650
2017150
201810
201970
2020130
202170
2022120
2023160
2024140
2025160
2026110
FIG. 1 — Lineage of K060282, 2000–2026Source: 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 HAW? 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 HAW device

  1. #1 K253856 Geniant Cranial (Navigated Neurosurgical…score 15.0 · 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? (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
*K031196Surgetics Ortho Kneelogics Navigation System
Summary page 1
…tem Common/Usual Name: Image guided surgical navigation system Classification Name: Computed tomography x-ray system (accessory) 3· Equivalent to: K031196 - Surgetics ORTHO KNEELOGICS Navigation System 4. Intended Use: The TOTAL KNEE SURGETICS NAVIGATION SYSTEM is intended…
Praxim2005—

Also cleared against K031196: 2 other devices →

What descends from it? (147)

See all 147

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

NumberDeviceApplicantDecidedDescendants
K062146Uni Knee Surgetics Navigation SystemPraxim S.A200699
K091411Kneealign SystemOrthalign, Inc.200941
K093998Kneealign System with Reference SensorOrthalign, Inc.201040
K100742Exactech GPSBlue Ortho201020
K081232Total Knee Surgetics Navigation System with PraxitelesPraxim200818
K072267Total Hip Surgetics Navigation SystemPraxim S.A20070

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 6 years and passes through 3 companies; a new generation was cleared every 2.1 years on median.
  • None of the 6 ancestors has a recall.
  • Of its descendants, K062146 (Praxim S.A, 2006) has gone furthest, with 99 descendants of its own.
  • 2 other devices also cite its predicate K031196.

How does its category compare?

All HAW devices

HAW Neurological Stereotaxic Instrument: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · HAW

9in 2025

2007: 152008: 122009: 82010: 62011: 42012: 82013: 32014: 52015: 102016: 92017: 72018: 62019: 102020: 52021: 92022: 72023: 142024: 72025: 92026 (partial year): 5
2007high 15 (2007) · low 3 (2013)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HAW

163in 2025

2007: 107 days median2008: 112 days median2009: 221 days median2010: 138 days median2011: 66 days median2012: 178 days median2013: 172 days median2014: 238 days median2015: 232 days median2016: 175 days median2017: 226 days median2018: 112 days median2019: 147 days median2020: 88 days median2021: 168 days median2022: 128 days median2023: 142 days median2024: 107 days median2025: 163 days median2026 (partial year): 162 days median
2007high 238 (2014) · low 66 (2011)2026

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

Recalls per year · HAW

2in 2025

2007: 22008: 102009: 62010: 282011: 52012: 42013: 6, 1 Class I2014: 52015: 32016: 52017: 22018: 2, 2 Class I2019: 4, 1 Class I2020: 12021: 4, 2 Class I2022: 12023: 4, 1 Class I2024: 2, 2 Class I2025: 22026 (partial year): 6
2007high 28 (2010) · low 1 (2020)2026

Class I (9 since 2007) Class II/III not classified

Adverse event reports per year · HAW

3,425in 2025

2007: 492008: 532009: 962010: 2992011: 1,7252012: 9862013: 1,2902014: 1,6062015: 1,7672016: 1,8282017: 3,5052018: 4,4392019: 6,0622020: 3,4802021: 2,8272022: 1,9292023: 2,5102024: 3,7552025: 3,425
2007high 6,062 (2019) · low 49 (2007)2025

MAUDE reports naming product code HAW, 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
200715107249
2008121121053
20098221696
2010613828299
201146651,725
201281784986
201331726 (1)1,290
2014523851,606
20151023231,767
2016917551,828
2017722623,505
201861122 (2)4,439
2019101474 (1)6,062
202058813,480
202191684 (2)2,827
2022712811,929
2023141424 (1)2,510
202471072 (2)3,755
2025916323,425
202651626—

What is it indicated for?

The TOTAL KNEE SURGETICS Navigation System is intended for use during stereotaxic surgery to aid the surgeon in locating anatomical structures and aligning and the endoprostheses with the anatomical structures.

It is specifically indicated for:

Total Knee Arthroplasty

Indications for use as stated in the FDA summary.

Also cleared against K031196

2 other devices cite the same predicate.

  • K062146Uni Knee Surgetics Navigation SystemPraxim S.A · 2006
  • K053542Surgetics Ortho Osteologics Navigation SystemPraxim S.A · 2006

More from Praxim S.A

4 FDA decisions under this applicant name. See the company

  • K072267Total Hip Surgetics Navigation SystemPraxim S.A · 2007
  • K062146Uni Knee Surgetics Navigation SystemPraxim S.A · 2006
  • K053542Surgetics Ortho Osteologics Navigation SystemPraxim S.A · 2006

Recent decisions in HAW

The HAW category page

  • K262214Disposable Reflective Marker Spheres (AM-BK115S, AM-BL130S)Guangzhou Aimooe Technology Co., Ltd. · 2026
  • K253856Geniant Cranial (Navigated Neurosurgical Positioning Robot)Koh Young Technology, Inc. · 2026
  • K261932Leksell® Vantage Stereotactic SystemElekta Solutions AB · 2026
  • K253663Zeta Navigation SystemZeta Surgical, Inc. · 2026
  • K253379Stealth AXiS Cranial clinical applicationMedtronic Navigation, Inc. · 2026

https://510kreport.com/device/K060282 · printed Nov 4, 2026

Cite this page

510(k) Report. “K060282: Total Knee Surgetics Navigation System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K060282

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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