510(k) · Cleared
ClearedOTS Hip
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Ortoma AB · OLO Orthopedic Stereotaxic Instrument
Cleared on Jul 1, 2026 as substantially equivalent to K250086 (Ortoma AB, 2025) after a 28-day review. Its family tree reaches back 11 generations to 1999.
- Decided
- Jul 1, 2026
- Review
- 28 days
- Class
- Class II
- Product code
- OLO
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 11 generations to K983831 (1999). 39 ancestors in all. No later device cites it as a predicate yet.
- Root · 11 generations backK983831 VECTORVISION2Brainlab AG · 1999
- 7 generations between
- 3 generations backK181449 Ortoma Treatment Solution - OTSOrtoma AB · 2018
- 2 generations backK232140 OTS HipOrtoma AB · 2024 · Recalled
- 1 generation backK250086 OTS HipOrtoma AB · 2025 · Recalled
- This deviceK261852 OTS HipOrtoma AB · 2026
Show all 11 generations
- Root · 11 generations backK983831 VECTORVISION2Brainlab AG · 1999
- 10 generations backK014256 Kolibri Igs SystemsBrainlab AG · 2002
- 9 generations backK031770 CI TKR/UkrBrainlab AG · 2003
- 8 generations backK041899 Vectorvision Uni-KneeBrainlab AG · 2004
- 7 generations backK052966 CI Knee, CI MI TKRBrainlab AG · 2006
- 6 generations backK073615 Brainlab Knee Essential, Brainlab Knee Unlimited CI Knee, CI Knee…Brainlab AG · 2008
- 5 generations backK102990 Brainlab KneeBrainlab AG · 2011 · Recalled
- 4 generations backK122011 Navigation Software Hip-Universal; Navigation Software Hip…Brainlab AG · 2012 · Recalled
- 3 generations backK181449 Ortoma Treatment Solution - OTSOrtoma AB · 2018
- 2 generations backK232140 OTS HipOrtoma AB · 2024 · Recalled
- 1 generation backK250086 OTS HipOrtoma AB · 2025 · Recalled
- This deviceK261852 OTS HipOrtoma AB · 2026
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −11 | K983831 | VECTORVISION2 | Brainlab AG | 1999 | — |
| −10 | K014256 | Kolibri Igs Systems | Brainlab AG | 2002 | — |
| −9 | K031770 | CI TKR/Ukr | Brainlab AG | 2003 | — |
| −8 | K041899 | Vectorvision Uni-Knee | Brainlab AG | 2004 | — |
| −7 | K052966 | CI Knee, CI MI TKR | Brainlab AG | 2006 | — |
| −6 | K073615 | Brainlab Knee Essential, Brainlab Knee Unlimited CI Knee, CI Knee Unlimited | Brainlab AG | 2008 | — |
| −5 | K102990 | Brainlab Knee | Brainlab AG | 2011 | 1 |
| −4 | K122011 | Navigation Software Hip-Universal; Navigation Software Hip THR-Aesculap | Brainlab AG | 2012 | 1 |
| −3 | K181449 | Ortoma Treatment Solution - OTS | Ortoma AB | 2018 | — |
| −2 | K232140 | OTS Hip | Ortoma AB | 2024 | 1 |
| −1 | K250086 | OTS Hip | Ortoma AB | 2025 | 1 |
| 0 (this device) | K261852 | OTS Hip | Ortoma AB | 2026 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2000 | 2 | 0 |
| 2001 | 6 | 0 |
| 2002 | 6 | 0 |
| 2004 | 1 | 0 |
| 2005 | 4 | 0 |
| 2006 | 4 | 0 |
| 2007 | 2 | 0 |
| 2009 | 1 | 0 |
| 2011 | 2 | 0 |
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 K240662 Spine Guidance Software (version 5.0); Xia 3/…score 23.7 · 15 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K250086 | OTS HipSummary page 5…Stereotaxic Instrument Classification Name: 21 CFR Section 882.4560, Stereotaxic Instrument Regulatory Class: II Product Code: OLO Predicate Devices Ortoma AB, OTS Hip (K250086) K261852 - Page 1 of 9… | 2025 |
What descends from it?
No later submission names this one as a predicate yet.
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 27 years and passes through 2 companies; a new generation was cleared every 1.6 years on median.
- 7 of the 39 ancestors have a recall of any class.
How does its category compare?
All OLO devicesOLO Orthopedic Stereotaxic Instrument: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, this device’s year, is highlighted.
FDA decisions per year · OLO
40in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · OLO
119in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · OLO
1in 2025
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · OLO
3,306in 2025
MAUDE reports naming product code OLO, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 1 |
| 2009 | 11 | 126 | 0 | 4 |
| 2010 | 9 | 113 | 1 | 4 |
| 2011 | 11 | 138 | 1 | 10 |
| 2012 | 7 | 129 | 1 | 60 |
| 2013 | 7 | 137 | 0 | 36 |
| 2014 | 10 | 119 | 3 | 245 |
| 2015 | 10 | 176 | 2 | 466 |
| 2016 | 14 | 120 | 3 | 750 |
| 2017 | 33 | 91 | 2 | 1,076 |
| 2018 | 24 | 97 | 1 | 1,230 |
| 2019 | 35 | 95 | 1 | 1,585 |
| 2020 | 34 | 89 | 6 | 2,746 |
| 2021 | 28 | 91 | 0 | 1,696 |
| 2022 | 40 | 89 | 5 | 1,568 |
| 2023 | 45 | 90 | 7 (1) | 1,493 |
| 2024 | 44 | 90 | 4 | 2,353 |
| 2025 | 40 | 119 | 1 | 3,306 |
| 2026 | 42 | 109 | 6 | — |
What is it indicated for?
OTS Hip is indicated to enable planning of orthopedic surgical procedures based on CT and X-Ray medical imaging data of the patient anatomy. It is an intraoperative image-guided localization system that enables navigated surgery. It links a freehand probe, tracked by a passive marker sensor system, to virtual computer image space on a patient's preoperative image data being processed by the OTS platform. The system is indicated for orthopedic hip…
Read the full statement (139 words)
OTS Hip is indicated to enable planning of orthopedic surgical procedures based on CT and X-Ray medical imaging data of the patient anatomy. It is an intraoperative image-guided localization system that enables navigated surgery. It links a freehand probe, tracked by a passive marker sensor system, to virtual computer image space on a patient's preoperative image data being processed by the OTS platform.
The system is indicated for orthopedic hip surgical procedures where a reference to a rigid anatomical structure, such as the pelvis, can be identified relative to a system generated model of the anatomy. The system aids the surgeon to accurately navigate a compatible prosthesis to the preoperatively planned position.
The system is designed for orthopedic surgical procedures including:
- Pre-operative planning of total hip arthroplasty (THA)
- Intraoperative navigated surgery for THA using a posterior approach
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K261852 · printed Nov 6, 2026
Cite this page
510(k) Report. “K261852: OTS Hip.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K261852
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Record history
- FDA decision record loaded Oct 30, 2026
- Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026