510(k) · Cleared
ClearedFusion Compact Navigation System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Medtronic Navigation, Inc. · PGW Ear, Nose, And Throat Stereotaxic Instrument
Cleared on Feb 18, 2016 as substantially equivalent to K001284 (Medtronic Surgical Navigation Technologies, 2000) after a 101-day review. Its family tree reaches back 1 generation to 2000. 4 later devices descend from it.
- Decided
- Feb 18, 2016
- Review
- 101 days
- Class
- Class II
- Product code
- PGW
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K001284 (2000). 4 later devices descend from it, 2 citing it directly.
- Root · 1 generation backK001284 Stealthstation System Goldeneye Micro-Magnetic Tracking SystemMedtronic Surgical Navigation Technologies · 2000 · Recalled
- This deviceK153247 Fusion Compact Navigation SystemMedtronic Navigation, Inc. · 2016
- Descendant · cites it directly · 3 of its ownK170018 StealthStationTM S8 ENT SoftwareMedtronic Navigation, Inc. · 2017
- Descendant · cites it directly · 2 of its ownK200723 StealthStation FlexENT (9736242), StealthStation S8 ENT Software…Medtronic Navigation, Inc. · 2020
- Descendant · 2 generations on · 0 of its ownK253395 Stealth AXiS™ ENT clinical applicationMedtronic Navigation, Inc. · 2026
- Descendant · 2 generations on · 0 of its ownK223734 ENT EMBrainlab AG · 2023
Most influential descendants
Showing 4 of 4 · See all- K170018StealthStationTM S8 ENT SoftwareMedtronic Navigation, Inc. · 2017 · cites it directly3descendants
- K200723StealthStation FlexENT (9736242), StealthStation S8 ENT Software (9735762)Medtronic Navigation, Inc. · 2020 · cites it directly2descendants
- K253395Stealth AXiS™ ENT clinical applicationMedtronic Navigation, Inc. · 2026 · 2 generations on0descendants
- K223734ENT EMBrainlab AG · 2023 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K001284 | Stealthstation System Goldeneye Micro-Magnetic Tracking System | Medtronic Surgical Navigation Technologies | 2000 | 28 |
| 0 (this device) | K153247 | Fusion Compact Navigation System | Medtronic Navigation, Inc. | 2016 | — |
| +1 | K170018 | StealthStationTM S8 ENT Software | Medtronic Navigation, Inc. | 2017 | — |
| +1 | K200723 | StealthStation FlexENT (9736242), StealthStation S8 ENT Software (9735762) | Medtronic Navigation, Inc. | 2020 | — |
| +2 | K253395 | Stealth AXiS™ ENT clinical application | Medtronic Navigation, Inc. | 2026 | — |
| +2 | K223734 | ENT EM | Brainlab AG | 2023 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2017 | 1 | 0 |
| 2020 | 1 | 0 |
| 2023 | 1 | 0 |
| 2026 | 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.
Planning a device in PGW? 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 PGW device
- #1 K261540 Cube 4D Navigation System, VirtuEye Proscore 13.0 · 6 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 |
|---|---|---|---|
| * | K001284 | Stealthstation System Goldeneye Micro-Magnetic Tracking SystemSummary page 4…ification: Class II Product Code: PGW Classification Name: 882.4560 – Stereotaxic Instrument Predicate Device: K001284 – StealthStation System GoldenEye Micro-Magnetic Tracking System Option Device Description:… | 2000 |
What descends from it? (4)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
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?
How does its category compare?
All PGW devicesPGW Ear, Nose, And Throat Stereotaxic Instrument: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, this device’s year, is highlighted.
FDA decisions per year · PGW
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · PGW
100in 2020
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · PGW
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · PGW
220in 2025
MAUDE reports naming product code PGW, 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 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 4 | 116 | 0 | 7 |
| 2015 | 1 | — | 0 | 14 |
| 2016 | 9 | 115 | 0 | 33 |
| 2017 | 4 | 125 | 0 | 42 |
| 2018 | 2 | — | 0 | 96 |
| 2019 | 1 | — | 3 | 247 |
| 2020 | 8 | 100 | 0 | 161 |
| 2021 | 1 | — | 1 | 190 |
| 2022 | 2 | — | 0 | 166 |
| 2023 | 2 | — | 1 | 200 |
| 2024 | 0 | — | 0 | 274 |
| 2025 | 1 | — | 1 | 220 |
| 2026 | 3 | 65 | 0 | — |
What is it indicated for?
The Medtronic Fusion Compact computer-assisted surgery system and its associated applications are intended as an aid
for precisely locating anatomical structures in either open or percutaneous ENT procedures. Their use is indicated for any
medical condition in which the use of stereotactic surgery may be appropriate, and where reference to a rigid anatomical
structure, such as the skull, can be identified relative to images of the anatomy.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K153247 · printed Nov 3, 2026
Cite this page
510(k) Report. “K153247: Fusion Compact Navigation System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K153247
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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