PMA · Approved
Recalled · Class II · 2017Defender II Model 9201 Implantable Cardioverter Defibrillator
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
MicroPort CRM USA, Inc. · MRM Defibrillator, Implantable, Dual-Chamber
Approved on Sep 15, 1999 through premarket approval, which rests on the device’s own clinical evidence after a 271-day review. It has been recalled 4 times.
- Decided
- Sep 15, 1999
- Review
- 271 days
- Class
- Class III
- Product code
- MRM
- Recalls
- 4
PMA approvals rest on their own clinical evidence and do not claim a predicate, so this family tree starts here.
P980049 has 145 supplements since 2000: 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 |
|---|---|
| 2000 | 3 |
| 2001 | 3 |
| 2002 | 1 |
| 2003 | 4 |
| 2004 | 6 |
| 2005 | 2 |
| 2006 | 3 |
| 2007 | 4 |
| 2008 | 16 |
| 2009 | 8 |
| 2010 | 9 |
| 2011 | 5 |
| 2012 | 11 |
| 2013 | 11 |
| 2014 | 16 |
| 2015 | 7 |
| 2016 | 11 |
| 2017 | 4 |
| 2018 | 6 |
| 2019 | 2 |
| 2020 | 4 |
| 2021 | 3 |
| 2022 | 1 |
| 2023 | 3 |
| 2025 | 2 |
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 MRM? 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)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Jul 24, 2017 | Class II | Z-3232-2017 | Software design | There is a possibility of overconsumption of certain PLATINIUM Implantable Cardiac Defibrillators (ICDs) and Cardiac ResynchronizationTherapy Defibrillators (CRT-Ds) following an ElectroStatic Discharge (ESD) during the implant surgery or… |
| Jul 24, 2017 | Class II | Z-3231-2017 | Software design | There is a possibility of overconsumption of certain PLATINIUM Implantable Cardiac Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) following an ElectroStatic Discharge (ESD) during the implant surgery… |
| Jul 24, 2017 | Class II | Z-3229-2017 | Software design | There is a possibility of overconsumption of certain PLATINIUM Implantable Cardiac Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) following an ElectroStatic Discharge (ESD) during the implant surgery… |
| Jul 24, 2017 | Class II | Z-3228-2017 | Software design | There is a possibility of overconsumption of certain PLATINIUM Implantable Cardiac Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) following an ElectroStatic Discharge (ESD) during the implant surgery… |
No ancestor or descendant has a Class I recall.
How does its category compare?
All MRM devicesMRM Defibrillator, Implantable, Dual-Chamber: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · MRM
23in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · MRM
Too few MRM 510(k)s in any year since 2007 to give a median.
Recalls per year · MRM
1in 2013
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · MRM
451in 2025
MAUDE reports naming product code MRM, 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 | 12 | — | 1 | 34 |
| 2008 | 32 | — | 0 | 77 |
| 2009 | 20 | — | 0 | 243 |
| 2010 | 28 | — | 0 | 581 |
| 2011 | 16 | — | 1 | 458 |
| 2012 | 19 | — | 0 | 427 |
| 2013 | 24 | — | 1 | 397 |
| 2014 | 20 | — | 0 | 320 |
| 2015 | 18 | — | 0 | 293 |
| 2016 | 20 | — | 0 | 384 |
| 2017 | 24 | — | 0 | 415 |
| 2018 | 19 | — | 0 | 372 |
| 2019 | 20 | — | 0 | 345 |
| 2020 | 23 | — | 0 | 316 |
| 2021 | 18 | — | 0 | 575 |
| 2022 | 9 | — | 0 | 505 |
| 2023 | 20 | — | 0 | 551 |
| 2024 | 19 | — | 0 | 514 |
| 2025 | 23 | — | 0 | 451 |
| 2026 | 25 | — | 0 | — |
https://510kreport.com/device/P980049 · printed Nov 6, 2026
Cite this page
510(k) Report. “P980049: Defender II Model 9201 Implantable Cardioverter Defibrillator.” Lineage record from FDA PMA data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/P980049
Report an extraction error
Are you the manufacturer?
Record history
- FDA decision record loaded May 2, 2026
- Page last updated Nov 3, 2026