PMA · Approved
ApprovedMelody Transcatheter Pulmonary Valve (TPV), Ensemble Transcatheter Valve Delivery System (DS)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Medtronic, Inc. · NPV Pulmonary Valve Prosthesis Percutaneously Delivered
Approved on Jan 27, 2015 through premarket approval, which rests on the device’s own clinical evidence after a 159-day review.
- Decided
- Jan 27, 2015
- Review
- 159 days
- Class
- Class f
- Product code
- NPV
- Recalls
- None
PMA approvals rest on their own clinical evidence and do not claim a predicate, so this family tree starts here.
P140017 has 33 supplements since 2015: changes to the approved device, its labelling or its manufacturing, each approved separately.
PMA supplements approved per year
View FIG. 1 as a table
| Year | Supplements approved |
|---|---|
| 2015 | 1 |
| 2016 | 3 |
| 2017 | 5 |
| 2018 | 2 |
| 2019 | 4 |
| 2021 | 1 |
| 2022 | 5 |
| 2023 | 2 |
| 2024 | 3 |
| 2025 | 3 |
| 2026 | 4 |
Sources: FDA PMA database (decision fields and supplements), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in NPV? 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?
PMA decisions do not claim a predicate device.
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.
How does its category compare?
All NPV devicesNPV Pulmonary Valve Prosthesis Percutaneously Delivered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.
FDA decisions per year · NPV
22in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · NPV
Too few NPV 510(k)s in any year since 2007 to give a median.
Recalls per year · NPV
1in 2022
Class I (2 since 2007) Class II/III not classified
Adverse event reports per year · NPV
329in 2025
MAUDE reports naming product code NPV, 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 | 20 |
| 2011 | 0 | — | 0 | 41 |
| 2012 | 0 | — | 0 | 25 |
| 2013 | 0 | — | 0 | 36 |
| 2014 | 0 | — | 0 | 48 |
| 2015 | 2 | — | 0 | 72 |
| 2016 | 3 | — | 0 | 66 |
| 2017 | 5 | — | 0 | 96 |
| 2018 | 2 | — | 0 | 126 |
| 2019 | 4 | — | 0 | 143 |
| 2020 | 7 | — | 0 | 112 |
| 2021 | 16 | — | 0 | 153 |
| 2022 | 26 | — | 1 (1) | 191 |
| 2023 | 36 | — | 0 | 253 |
| 2024 | 19 | — | 0 | 325 |
| 2025 | 22 | — | 0 | 329 |
| 2026 | 24 | — | 1 (1) | — |
https://510kreport.com/device/P140017 · printed Nov 6, 2026
Cite this page
510(k) Report. “P140017: Melody Transcatheter Pulmonary Valve (TPV), Ensemble Transcatheter Valve Delivery System (DS).” Lineage record from FDA PMA data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/P140017
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Record history
- FDA decision record loaded May 2, 2026
- Page last updated Nov 3, 2026