FDA product code · Cardiovascular
Left Atrial Appendage Clip, Implantable
11 FDA decisions since 2018. 510(k) reviews decided 2021–2025 took a median of 30 days (half between 29 and 168). No recall names this code. The most-cited predicate is K210293, named by 3 later devices.
Intended to occlude the left atrial appendage.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly Download the data (CSV)
Twenty years of PZX at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.
FDA decisions per year · PZX
3so far in 2026, the most since 2007
2026 to Oct 25, outlined.
Median 510(k) review, days · PZX
179in 2026
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · PZX
No recall names PZX since 2007.
Adverse event reports per year · PZX
43in 2025
MAUDE reports naming product code PZX, 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 | 1 | — | 0 | 0 |
| 2019 | 1 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 1 | — | 0 | 10 |
| 2022 | 1 | — | 0 | 14 |
| 2023 | 2 | — | 0 | 9 |
| 2024 | 1 | — | 0 | 35 |
| 2025 | 1 | — | 0 | 43 |
| 2026 | 3 | 179 | 0 | — |
Planning a device in PZX? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportRelated product codes
Other codes under 21 CFR 878.4300.