510(k) · Cleared
ClearedImPACT
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Impact Applications, Inc. · POM Computerized Cognitive Assessment Aid For Concussion
Cleared on Feb 23, 2017 as substantially equivalent to DEN150037 (Impact Applications, Inc., 2016) after a 30-day review. Its family tree reaches back 1 generation to 2016. 3 later devices descend from it.
- Decided
- Feb 23, 2017
- Review
- 30 days
- Class
- Class II
- Product code
- POM
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to DEN150037 (2016). 3 later devices descend from it, 1 citing it directly.
- Root · 1 generation backDEN150037 ImPACT Computerized Neurocognitive Concussion Management AidImpact Applications, Inc. · 2016
- This deviceK170209 ImPACTImpact Applications, Inc. · 2017
- Descendant · cites it directly · 2 of its ownK181223 ImPACTImpact Applications, Inc. · 2018
- Descendant · 2 generations on · 1 of its ownK202485 ImPACT Version 4Impact Applications, Inc. · 2020
- Descendant · 3 generations on · 0 of its ownK231688 ImPACT Version 4Impact Applications, Inc. · 2023
Most influential descendants
Showing 3 of 3 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | DEN150037 | ImPACT Computerized Neurocognitive Concussion Management Aid | Impact Applications, Inc. | 2016 | — |
| 0 (this device) | K170209 | ImPACT | Impact Applications, Inc. | 2017 | — |
| +1 | K181223 | ImPACT | Impact Applications, Inc. | 2018 | — |
| +2 | K202485 | ImPACT Version 4 | Impact Applications, Inc. | 2020 | — |
| +3 | K231688 | ImPACT Version 4 | Impact Applications, Inc. | 2023 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2018 | 1 | 0 |
| 2020 | 1 | 0 |
| 2023 | 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 POM? 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 POM device
- #1 K241737 Sway System Sports Plusscore 9.2 · 2 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 |
|---|---|---|---|
| * | DEN150037 | ImPACT Computerized Neurocognitive Concussion Management AidSummary page 4…vice Classification: Class II Product Code: POM, 21 CFR 882.1471 Panel: Neurology Predicate Device: ImPACT, DEN150037 Reason for submission Device Modifications Indications for Use: ImPACT is intended for use as a computer-based neuroc… | 2016 |
What descends from it? (3)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K181223 | ImPACT | 2018 | 2 |
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 POM devicesPOM Computerized Cognitive Assessment Aid For Concussion: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.
FDA decisions per year · POM
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · POM
Too few POM 510(k)s in any year since 2007 to give a median.
Recalls per year · POM
No recall names POM since 2007.
Adverse event reports per year · POM
No MAUDE report names POM since 2007.
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 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 1 | — | 0 | 0 |
| 2017 | 2 | — | 0 | 0 |
| 2018 | 1 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 1 | — | 0 | 0 |
| 2021 | 1 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 1 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 1 | — | 0 | 0 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
ImPACT is intended for use as a computer-based neurocognitive test battery to aid in the assessment and management of concussion.
ImPACT is a neurocognitive test battery that provides healthcare professionals with objective measure of neurocognitive functioning as an assessment aid and in the management of concussion in individuals ages 12-59.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K170209 · printed Nov 6, 2026
Cite this page
510(k) Report. “K170209: ImPACT.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K170209
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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