MAUDE MDR 219270
- MDR report key
- 219270
- Report number
- 6000002-1999-00094
- Event key
- 0
- Event type
- 3
- Date of event
- 1998-03-07
- Date received
- 1999-04-16
- Adverse event
- 3
- Product problem
- 3
- Patients in event
- 0
- Reporter occupation
- 1
- Health professional
- 3
- Initial report to FDA
- 3
- Event location
- 3
Manufacturer Contact
- Report source
- M
- Manufacturer link flag
- Y
Devices
| Seq | Brand | Generic | Manufacturer | Product code | Model | Catalog | Lot | PMA | 510(k) | Implant | Evaluated | Availability |
|---|
| 1 | EDWARDS PERICARDIAL PATCH | PERICARDIAL PATCH | BAXTER HEALTHCARE CORP. | MFX | 4700 | NA | F60121A | | K833763 | N | R | N |
Patients
| Sequence | Received | Treatment | Outcome |
|---|
| 1 | 1999-04-16 | 0 | 1. D
|
Event Narratives
D
Patient 1
THIS PT REPORTEDLY EXPIRED DUE TO CARDIAC FAILURE. NO FURTHER INFO WAS PROVIDED.
Related GUDID Devices By Product Code
No records found.
Related PMN/PMA Records By Product Code
| Type | Submission | Product code | Device | Applicant | Decision date |
|---|
| 510(k) | K061727 | MFX | GORE PRECLUDE VESSEL GUARD | W. L. Gore & Associates, Inc. | 2006-08-07 |
| 510(k) | K960532 | MFX | PRECLUDE IMA SLEEVE | W. L. Gore & Associates, Inc. | 1996-05-23 |