510(k) Report

510(k) · Cleared

Cleared

Intellijoint Hip

K133759510(k) TraditionalCleared Jul 23, 2014224-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

Intellijoint Surgical, Inc. · OLO Orthopedic Stereotaxic Instrument

Cleared on Jul 23, 2014 as substantially equivalent to K110021 (Brainlab AG, 2011) and 1 other predicate after a 224-day review. Its family tree reaches back 7 generations to 2001. 10 later devices descend from it.

Decided
Jul 23, 2014
Review
224 days
Class
Class II
Product code
OLO
Recalls
None
Predicates
2

Its longest line of descent runs back 7 generations to K010612 (2001). 17 ancestors in all, the oldest K983831 (1999). 10 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2006: 2 other ancestors2002: 3 other ancestors2007: 1 other ancestor2001: 2 other ancestors2000: 1 other ancestor1999: 1 other ancestor2015: 1 descendant cleared2019: 2 descendants cleared2017: 3 descendants cleared2020: 1 descendant cleared2021: 1 descendant cleared2023: 1 descendant cleared2026: 1 descendant clearedK010612 · Vectorvision Knee · Brainlab AG · 2001K021306 · Vectorvision CT-Free Knee · Brainlab AG · 2002K040368 · Vectorvision Hip 3.0 · Brainlab AG · 2004K052213 · Navigation SW Hip 3.1 on CI · Brainlab AG · 2005K060468 · Vectorvision Hip · Brainlab AG · 2006K083483 · Brainlab Hip Unlimited, CI Hip Unlimited · Brainlab AG · 2009K110021 · Dash Hip · Brainlab AG · 20111995200020052010201520202025
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 2 other ancestors3 generations back: 5 other ancestors4 generations back: 2 other ancestors 1 generation forward: 2 descendants2 generations forward: 2 descendants3 generations forward: 3 descendants4 generations forward: 2 descendants5 generations forward: 1 descendant K110021 · Dash Hip · Brainlab AG · 2011K083483 · Brainlab Hip Unlimited, CI Hip Unlimited · Brainlab AG · 2009K060468 · Vectorvision Hip · Brainlab AG · 2006K052213 · Navigation SW Hip 3.1 on CI · Brainlab AG · 2005K040368 · Vectorvision Hip 3.0 · Brainlab AG · 2004K021306 · Vectorvision CT-Free Knee · Brainlab AG · 2002K010612 · Vectorvision Knee · Brainlab AG · 2001−50+5
  1. Root · 7 generations backK010612 Vectorvision KneeBrainlab AG · 2001
  2. 6 generations backK021306 Vectorvision CT-Free KneeBrainlab AG · 2002
  3. 5 generations backK040368 Vectorvision Hip 3.0Brainlab AG · 2004
  4. 4 generations backK052213 Navigation SW Hip 3.1 on CIBrainlab AG · 2005
  5. 3 generations backK060468 Vectorvision HipBrainlab AG · 2006
  6. 2 generations backK083483 Brainlab Hip Unlimited, CI Hip UnlimitedBrainlab AG · 2009
  7. 1 generation backK110021 Dash HipBrainlab AG · 2011
  8. This deviceK133759 Intellijoint HipIntellijoint Surgical, Inc. · 2014
  9. Descendant · cites it directly · 8 of its ownK151364 Intellijoint HIP (tm) SystemIntellijoint Surgical, Inc. · 2015
  10. Descendant · 2 generations on · 7 of its ownK162364 Intellijoint HIP Generation 2A SystemIntellijoint Surgical, Inc. · 2017
  11. Descendant · 3 generations on · 3 of its ownK171525 Intellijoint HIP Generation 2B SystemIntellijoint Surgical, Inc. · 2017
  12. Descendant · 4 generations on · 2 of its ownK191507 Intellijoint® Navigation SystemIntellijoint Surgical, Inc. · 2019 · Recalled
  13. Descendant · 3 generations on · 1 of its ownK193094 Naviswiss Hip Navigation SystemNaviswiss AG · 2020

Showing 5 of 10 descendants. See all descendants

Descendants cleared per year

2015: 12017: 32019: 22020: 12021: 12023: 12026: 1
2015high 3 (2017) · low 0 (2016)2026

Most influential descendants

Showing 5 of 10 · See all
  • K151364Intellijoint HIP (tm) SystemIntellijoint Surgical, Inc. · 2015 · cites it directly8descendants
  • K162364Intellijoint HIP Generation 2A SystemIntellijoint Surgical, Inc. · 2017 · 2 generations on7descendants
  • K171525Intellijoint HIP Generation 2B SystemIntellijoint Surgical, Inc. · 2017 · 3 generations on3descendants
  • K191507Intellijoint® Navigation SystemIntellijoint Surgical, Inc. · 2019 · 4 generations on2descendants
  • K193094Naviswiss Hip Navigation SystemNaviswiss AG · 2020 · 3 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K010612Vectorvision KneeBrainlab AG2001—
−6K021306Vectorvision CT-Free KneeBrainlab AG2002—
−5K040368Vectorvision Hip 3.0Brainlab AG2004—
−4K052213Navigation SW Hip 3.1 on CIBrainlab AG2005—
−3K060468Vectorvision HipBrainlab AG2006—
−2K083483Brainlab Hip Unlimited, CI Hip UnlimitedBrainlab AG2009—
−1K110021Dash HipBrainlab AG2011—
0 (this device)K133759Intellijoint HipIntellijoint Surgical, Inc.2014—
+1K151364Intellijoint HIP (tm) SystemIntellijoint Surgical, Inc.2015—
+2K162364Intellijoint HIP Generation 2A SystemIntellijoint Surgical, Inc.2017—
+3K171525Intellijoint HIP Generation 2B SystemIntellijoint Surgical, Inc.2017—
+4K191507Intellijoint® Navigation SystemIntellijoint Surgical, Inc.20192
+3K193094Naviswiss Hip Navigation SystemNaviswiss AG2020—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199910
200010
200120
200230
200620
200710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201510
201730
201920
202010
202110
202310
202610
FIG. 1 — Lineage of K133759, 2001–2026Source: 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 OLO? 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 OLO device

  1. #1 K240662 Spine Guidance Software (version 5.0); Xia 3/…score 23.7 · 15 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
*K110021Dash Hip
Summary page 1
…t HIP™ System described in this submission is substantially equivalent to the following predicates: Predicate Device Manufacturer 510(k) No. DASH Hip System BrainLAB AG K110021 StealthStation Imageless Hip Module | Medtronic K052623 5. Device Description The Intellijoint HIP™ System is an imageless opti…
Brainlab AG2011—
*K052623Imageless Hip Module for the Stealthstation System
Summary page 1
…lly equivalent to the following predicates: Predicate Device Manufacturer 510(k) No. DASH Hip System BrainLAB AG K110021 StealthStation Imageless Hip Module | Medtronic K052623 5. Device Description The Intellijoint HIP™ System is an imageless optical navigation system intended for orthopedic surgery. T…
Medtronic Navigation, Inc.2006—

Also cleared against K110021: 2 other devices →

What descends from it? (10)

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

NumberDeviceApplicantDecidedDescendants
K151364Intellijoint HIP (tm) SystemIntellijoint Surgical, Inc.20158
K182524GALILEO Spine Alignment Monitoring SystemMiRus, LLC20190

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 13 years and passes through 2 companies; a new generation was cleared every 1.8 years on median.
  • 2 of the 17 ancestors have a recall of any class.
  • Of its descendants, K151364 (Intellijoint Surgical, Inc., 2015) has gone furthest, with 8 descendants of its own.
  • 2 other devices also cite its predicate K110021.

How does its category compare?

All OLO devices

OLO Orthopedic Stereotaxic Instrument: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.

FDA decisions per year · OLO

40in 2025

2009: 112010: 92011: 112012: 72013: 72014: 102015: 102016: 142017: 332018: 242019: 352020: 342021: 282022: 402023: 452024: 442025: 402026 (partial year): 42
2007high 45 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OLO

119in 2025

2009: 126 days median2010: 113 days median2011: 138 days median2012: 129 days median2013: 137 days median2014: 119 days median2015: 176 days median2016: 120 days median2017: 91 days median2018: 97 days median2019: 95 days median2020: 89 days median2021: 91 days median2022: 89 days median2023: 90 days median2024: 90 days median2025: 119 days median2026 (partial year): 109 days median
2007high 176 (2015) · low 89 (2020)2026

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

Recalls per year · OLO

1in 2025

2010: 12011: 12012: 12014: 32015: 22016: 32017: 22018: 12019: 12020: 62022: 52023: 7, 1 Class I2024: 42025: 12026 (partial year): 6
2007high 7 (2023) · low 0 (2007)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · OLO

3,306in 2025

2008: 12009: 42010: 42011: 102012: 602013: 362014: 2452015: 4662016: 7502017: 1,0762018: 1,2302019: 1,5852020: 2,7462021: 1,6962022: 1,5682023: 1,4932024: 2,3532025: 3,306
2007high 3,306 (2025) · low 0 (2007)2025

MAUDE reports naming product code OLO, 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—01
20091112604
2010911314
201111138110
20127129160
20137137036
2014101193245
2015101762466
2016141203750
2017339121,076
2018249711,230
2019359511,585
2020348962,746
2021289101,696
2022408951,568
202345907 (1)1,493
2024449042,353
20254011913,306
2026421096—

What is it indicated for?

Intellijoint HIP™ is an infrared. computer-controlled localizer intended to provide intra-operative measurements to a surgeon to aid in selection and positioning of orthopedic implant system components, relative to anatomical structures and reference axes. Intellijoint HIP™ is indicated for patients undergoing orthopedic surgery where the use of stereotactic surgery is considered safe and effective, and where a reference to a rigid anatomical structure…

Read the full statement (105 words)

Intellijoint HIP™ is an infrared. computer-controlled localizer intended to provide intra-operative measurements to a surgeon to aid in selection and positioning of orthopedic implant system components, relative to anatomical structures and reference axes.

Intellijoint HIP™ is indicated for patients undergoing orthopedic surgery where the use of stereotactic surgery is considered safe and effective, and where a reference to a rigid anatomical structure, such as a long bone, can be identified relative to the anatomy. The system aids the surgeon in controlling leg length and offset discrepancies.

Example orthopedic surgical procedures include, but are not limited to:

- Total Hip Arthroplasty

- Minimally Invasive Hip Arthroplasty

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. “K133759: Intellijoint Hip.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K133759

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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