Brand Name | NURO |
Type of Device | STIMULATOR,PERIPHERAL NERVE,NON-IMPLANTED,FOR PELVIC FLOOR DYSFUNCTION |
Manufacturer (Section D) |
MEDTRONIC NEUROMODULATION |
800 53rd ave ne |
minneapolis MN 55421 1200 |
|
Manufacturer (Section G) |
MEDTRONIC NEUROMODULATION |
800 53rd ave ne |
|
minneapolis MN 55421 1200 |
|
Manufacturer Contact |
lisa
clark
|
7000 central avenue ne rcw215 |
minneapolis, MN 55432
|
7635263920
|
|
MDR Report Key | 6271294 |
MDR Text Key | 65539692 |
Report Number | 3007566237-2017-00232 |
Device Sequence Number | 1 |
Product Code |
NAM
|
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K132561 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
consumer |
Reporter Occupation |
Other
|
Type of Report
| Initial |
Report Date |
01/23/2017 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Health Professional
|
Device Model Number | 3533 |
Device Catalogue Number | 3533 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
No
|
Initial Date Manufacturer Received |
12/28/2016
|
Initial Date FDA Received | 01/23/2017 |
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Unknown
|
Patient Sequence Number | 1 |
Patient Outcome(s) |
Required Intervention;
|
|
|