510(k) · Cleared
ClearedClearpoint System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Surgivision, Inc. · ORR Neurological Stereotaxic Instrument, Real-Time Intraoperative Mri
Cleared on Jun 16, 2010 as substantially equivalent to K012719 (Image-Guided Neurologics, Inc., 2001) and 1 other predicate after an 84-day review. Its family tree reaches back 4 generations to 2003. 4 of the 21 devices in its family, counting itself, have a Class I recall. 12 later devices descend from it.
- Decided
- Jun 16, 2010
- Review
- 84 days
- Class
- Class II
- Product code
- ORR
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 4 generations to K031815 (2003). 8 ancestors in all, the oldest K001796 (2000). 12 later devices descend from it, 1 citing it directly. 4 of the 21 devices in this family, counting this one, have a Class I recall.
- Root · 4 generations backK031815 Intera-Sensation FamilyPhilips Medical Systems · 2003 · Recalled
- 3 generations backK041602 Panorama 1.0TPhilips Medical Systems North America, Inc. · 2004 · Recalled (Class I)
- 2 generations backK052078 Achieva, Intera and Panorama 1.0 Release 2-SeriesPhilips Medical Systems Nederland B.V. · 2005 · Recalled (Class I)
- 1 generation backK063559 Achieva, Intera and Panorama 1.0T, Release 2.5Philips Medical Systems · 2007 · Recalled (Class I)
- This deviceK100836 Clearpoint SystemSurgivision, Inc. · 2010
- Descendant · cites it directly · 11 of its ownK111073 Surgivision Inc. Clearpoint SystemSurgi-Vision, Inc. · 2011
- Descendant · 2 generations on · 10 of its ownK142505 ClearPoint SystemMri Interventions, Inc. · 2015
- Descendant · 3 generations on · 9 of its ownK160434 ClearPoint SystemMri Interventions, Inc. · 2016
- Descendant · 4 generations on · 8 of its ownK171257 ClearPoint SystemMri Interventions, Inc. · 2017
- Descendant · 5 generations on · 7 of its ownK181195 ClearPoint SystemMri Interventions, Inc. · 2018
Showing 5 of 12 descendants. See all descendants
Descendants cleared per year
Class I recalls in this family
Most influential descendants
Showing 5 of 12 · See all- K111073Surgivision Inc. Clearpoint SystemSurgi-Vision, Inc. · 2011 · cites it directly11descendants
- K142505ClearPoint SystemMri Interventions, Inc. · 2015 · 2 generations on10descendants
- K160434ClearPoint SystemMri Interventions, Inc. · 2016 · 3 generations on9descendants
- K171257ClearPoint SystemMri Interventions, Inc. · 2017 · 4 generations on8descendants
- K181195ClearPoint SystemMri Interventions, Inc. · 2018 · 5 generations on7descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K031815 | Intera-Sensation Family | Philips Medical Systems | 2003 | 3 |
| −3 | K041602 | Panorama 1.0T | Philips Medical Systems North America, Inc. | 2004 | Class I |
| −2 | K052078 | Achieva, Intera and Panorama 1.0 Release 2-Series | Philips Medical Systems Nederland B.V. | 2005 | Class I |
| −1 | K063559 | Achieva, Intera and Panorama 1.0T, Release 2.5 | Philips Medical Systems | 2007 | Class I |
| 0 (this device) | K100836 | Clearpoint System | Surgivision, Inc. | 2010 | — |
| +1 | K111073 | Surgivision Inc. Clearpoint System | Surgi-Vision, Inc. | 2011 | — |
| +2 | K142505 | ClearPoint System | Mri Interventions, Inc. | 2015 | — |
| +3 | K160434 | ClearPoint System | Mri Interventions, Inc. | 2016 | — |
| +4 | K171257 | ClearPoint System | Mri Interventions, Inc. | 2017 | — |
| +5 | K181195 | ClearPoint System | Mri Interventions, Inc. | 2018 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2000 | 1 | 0 |
| 2001 | 2 | 0 |
| 2005 | 1 | 1 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2011 | 1 | 0 |
| 2015 | 1 | 0 |
| 2016 | 1 | 0 |
| 2017 | 1 | 0 |
| 2018 | 1 | 0 |
| 2020 | 1 | 0 |
| 2021 | 1 | 0 |
| 2022 | 2 | 0 |
| 2023 | 2 | 0 |
| 2025 | 1 | 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.
4 devices in this family have a Class I recall. A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K012719 | Navigus II MR | 2001 |
| * | K063559 | Achieva, Intera and Panorama 1.0T, Release 2.5Summary page 1…uided Neurologics, Inc. Navigus 1I MR Trajectory Guide (KO 12719) Philips Medical Systems software package for the Achieva, Intera and Panorama MR Systems (K063559) Intended Use!/ Indications for Use The ClearPoint System is intended to provide stereotactic guidance for the placemen… | 2007 |
What descends from it? (12)
See all 121 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K111073 | Surgivision Inc. Clearpoint System | 2011 | 11 |
Has anything in its family been recalled? (4 Class I)
No FDA recall names this device.
Relatives with a Class I recall
Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.
- K063559Achieva, Intera and Panorama 1.0T, Release 2.5Philips Medical Systems · 2007 · Direct predicate · ◆ on the line of descent in FIG. 11 Class I recall
- K052078Achieva, Intera and Panorama 1.0 Release 2-SeriesPhilips Medical Systems Nederland B.V. · 2005 · 2 generations back · ◆ on the line of descent in FIG. 11 Class I recall
- K043147Achieva FamilyPhilips Medical Systems North America Co. · 2005 · 2 generations back · ◆ in the 2005 ancestors bar of FIG. 13 Class I recalls
- K041602Panorama 1.0TPhilips Medical Systems North America, Inc. · 2004 · 2 generations back · ◆ on the line of descent in FIG. 11 Class I recall
What does this lineage say?
- The line of descent spans 7 years and passes through 4 companies; a new generation was cleared every 1.3 years on median.
- 7 of the 8 ancestors have a recall of any class; 4 have a Class I recall.
- Of its descendants, K111073 (Surgi-Vision, Inc., 2011) has gone furthest, with 11 descendants of its own.
How does its category compare?
All ORR devicesORR Neurological Stereotaxic Instrument, Real-Time Intraoperative Mri: FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, this device’s year, is highlighted.
FDA decisions per year · ORR
1in 2018
2026 to Oct 25, outlined.
Median 510(k) review, days · ORR
Too few ORR 510(k)s in any year since 2007 to give a median.
Recalls per year · ORR
No recall names ORR since 2007.
Adverse event reports per year · ORR
1in 2022
MAUDE reports naming product code ORR, 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 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 1 | — | 0 | 0 |
| 2011 | 1 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 2 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 1 | — | 0 | 1 |
| 2018 | 1 | — | 0 | 2 |
| 2019 | 0 | — | 0 | 1 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 1 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The ClearPoint System is intended to provide stereotactic guidance for the placement and operation of instruments or devices during planning and operation of neurological procedures within the MRI environment and in conjunction with MR imaging. The ClearPoint System is intended as an integral part of procedures that have traditionally used stereotactic methodology. These procedures include biopsies, catheter and electrode insertion. The System is intended for use only with 1.5 Tesla MRI scanners.
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/K100836 · printed Nov 5, 2026
Cite this page
510(k) Report. “K100836: Clearpoint System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K100836
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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