PMA · Approved
ApprovedBAROSTIM NEO Implantable Pulse Generator (IPG), BAROSTIM NEO Carotid Sinus Lead (CSL) Kit, Programmer System, Carotid Le
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Cvrx, Inc. · DSR Stimulator, Carotid Sinus Nerve
Approved on Jan 11, 2024 through premarket approval, which rests on the device’s own clinical evidence after a 29-day review.
- Decided
- Jan 11, 2024
- Review
- 29 days
- Class
- Class III
- Product code
- DSR
- Recalls
- None
PMA approvals rest on their own clinical evidence and do not claim a predicate, so this family tree starts here.
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 DSR? 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 DSR devicesDSR Stimulator, Carotid Sinus Nerve: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.
FDA decisions per year · DSR
3in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · DSR
Too few DSR 510(k)s in any year since 2007 to give a median.
Recalls per year · DSR
No recall names DSR since 2007.
Adverse event reports per year · DSR
136in 2025
MAUDE reports naming product code DSR, 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 | 1 |
| 2016 | 0 | — | 0 | 1 |
| 2017 | 0 | — | 0 | 3 |
| 2018 | 0 | — | 0 | 1 |
| 2019 | 1 | — | 0 | 1 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 1 | — | 0 | 5 |
| 2022 | 6 | — | 0 | 24 |
| 2023 | 3 | — | 0 | 60 |
| 2024 | 2 | — | 0 | 93 |
| 2025 | 3 | — | 0 | 136 |
| 2026 | 0 | — | 0 | — |
https://510kreport.com/device/P180050/S012 · printed Nov 6, 2026
Cite this page
510(k) Report. “P180050/S012: BAROSTIM NEO Implantable Pulse Generator (IPG), BAROSTIM NEO Carotid Sinus Lead (CSL) Kit, Programmer System, Carotid Le.” Lineage record from FDA PMA data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/P180050/S012
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Record history
- FDA decision record loaded May 2, 2026
- Page last updated Nov 3, 2026