De Novo · Granted
GrantedShortCut
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Pi-Cardia, Ltd. · SCZ Percutaneous Catheter For Cutting Or Splitting Heart Valve Leaflets Concomitant To Transcatheter Valve Procedures
Granted on Sep 27, 2024 as a new device type through De Novo after a 163-day review. 1 later device descends from it.
- Decided
- Sep 27, 2024
- Review
- 163 days
- Class
- Class II
- Product code
- SCZ
- Recalls
- None
1 later device descends from it, 1 citing it directly.
- This deviceDEN240017 ShortCutPi-Cardia, Ltd. · 2024
- Descendant · cites it directly · 0 of its ownK252592 TELLTALE Electrosurgical Guidewire SystemTelltale, LLC · 2025
Most influential descendants
Showing 1 of 1 · See all- K252592TELLTALE Electrosurgical Guidewire SystemTelltale, LLC · 2025 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | DEN240017 | ShortCut | Pi-Cardia, Ltd. | 2024 | — |
| +1 | K252592 | TELLTALE Electrosurgical Guidewire System | Telltale, LLC | 2025 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2025 | 1 | 0 |
Sources: FDA De Novo 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 SCZ? 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
Does it have a predicate?
De Novo decisions do not claim a predicate device.
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K252592 | TELLTALE Electrosurgical Guidewire System | 2025 | 0 |
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?
- Of its descendants, K252592 (Telltale, LLC, 2025) has gone furthest, with 0 descendants of its own.
How does its category compare?
All SCZ devicesSCZ Percutaneous Catheter For Cutting Or Splitting Heart Valve Leaflets Concomitant To Transcatheter Valve Procedures: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.
FDA decisions per year · SCZ
1in 2024
2026 to Oct 25, outlined.
Median 510(k) review, days · SCZ
Too few SCZ 510(k)s in any year since 2007 to give a median.
Recalls per year · SCZ
1so far in 2026, the most since 2007
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · SCZ
7in 2025
MAUDE reports naming product code SCZ, 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 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 1 | — | 0 | 0 |
| 2025 | 0 | — | 0 | 7 |
| 2026 | 0 | — | 1 | — |
What is it indicated for?
ShortCut is indicated for use as a splitting device of bioprosthetic aortic valve leaflets to facilitate
valve-in-valve procedures for patients at risk of coronary obstruction.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/DEN240017 · printed Nov 6, 2026
Cite this page
510(k) Report. “DEN240017: ShortCut.” Lineage record from FDA De Novo data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/DEN240017
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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