510(k) · Cleared
ClearedAscendra Balloon Aortic Valvaloplasty Catheter
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Edwards Lifesciences · OZT Balloon Aortic Valvuloplasty
Cleared on Oct 29, 2014 as substantially equivalent to K121083 (Loma Vista Medical, 2012) and 1 other predicate after a 79-day review. Its family tree reaches back 1 generation to 2012.
- Decided
- Oct 29, 2014
- Review
- 79 days
- Class
- Class II
- Product code
- OZT
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 1 generation to K122012 (2012). 2 ancestors in all. No later device cites it as a predicate yet.
- Root · 1 generation backK122012 Z-Med Z-Med IINuMED, Inc. · 2012
- This deviceK142199 Ascendra Balloon Aortic Valvaloplasty CatheterEdwards Lifesciences · 2014
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K122012 | Z-Med Z-Med II | NuMED, Inc. | 2012 | — |
| 0 (this device) | K142199 | Ascendra Balloon Aortic Valvaloplasty Catheter | Edwards Lifesciences | 2014 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2012 | 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 OZT? 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 OZT device
- #1 K253855 KardiaPSI Balloon Catheterscore 11.3 · 1 generation · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin 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 |
|---|---|---|---|
| * | K121083 | True Dilatation Percutaneous Transluminal Valvuloplasty Catheter, 20MM X 4.5CM, True…Summary page 4…CFR 870.1255, Product Code OZT Predicate Device(s): Loma Vista Medical (BARD) TRUE Dilation Balloon Valvuloplasty Catheter (K121083) NuMed Z-MED and Z-MED II™ Balloon Aortic Valvuloplasty Catheter (K122012) Device… | 2012 |
| * | K122012 | Z-Med Z-Med IISummary page 4…oon Valvuloplasty Catheter (K121083) NuMed Z-MED and Z-MED II™ Balloon Aortic Valvuloplasty Catheter (K122012) Device Description: The Edwards Ascendra Balloon Aortic Valvuloplasty Catheter is used for balloon aortic valvuloplasty. The d… | 2012 |
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?
- 1 of the 2 ancestors has a recall of any class.
- 2 other devices also cite its predicate K121083.
How does its category compare?
All OZT devicesOZT Balloon Aortic Valvuloplasty: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.
FDA decisions per year · OZT
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · OZT
115in 2015
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · OZT
No recall names OZT since 2007.
Adverse event reports per year · OZT
34in 2025
MAUDE reports naming product code OZT, 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 | 3 | — | 0 | 0 |
| 2013 | 3 | 80 | 0 | 29 |
| 2014 | 4 | 79 | 0 | 17 |
| 2015 | 4 | 115 | 0 | 16 |
| 2016 | 1 | — | 0 | 9 |
| 2017 | 1 | — | 0 | 38 |
| 2018 | 0 | — | 0 | 31 |
| 2019 | 0 | — | 0 | 10 |
| 2020 | 0 | — | 0 | 11 |
| 2021 | 0 | — | 0 | 18 |
| 2022 | 1 | — | 0 | 33 |
| 2023 | 1 | — | 0 | 47 |
| 2024 | 1 | — | 0 | 38 |
| 2025 | 1 | — | 0 | 34 |
| 2026 | 2 | — | 0 | — |
What is it indicated for?
The Ascendra Balloon Aortic Valvuloplasty Catheter is indicated for balloon aortic valvuloplasty.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K142199 · printed Nov 3, 2026
Cite this page
510(k) Report. “K142199: Ascendra Balloon Aortic Valvaloplasty Catheter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K142199
Report an extraction error
Are you the manufacturer?
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