Brand Name | IMPLANTABLE NEUROSTIMULATOR |
Type of Device | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF |
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
woodward clark
|
7000 central avenue ne rcw215 |
minneapolis, MN 55432
|
7635263920
|
|
MDR Report Key | 9416503 |
MDR Text Key | 169248383 |
Report Number | 3007566237-2019-02477 |
Device Sequence Number | 1 |
Product Code |
LGW
|
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | P840001 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
consumer |
Reporter Occupation |
Non-Healthcare Professional
|
Type of Report
| Initial |
Report Date |
12/05/2019 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 12/05/2019 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Health Professional
|
Device Model Number | NEU_INS_STIMULATOR |
Device Catalogue Number | NEU_INS_STIMULATOR |
Was Device Available for Evaluation? |
No
|
Date Manufacturer Received | 11/29/2019 |
Is the Device Single Use? |
Yes
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Initial
|
Patient Sequence Number | 1 |
Patient Outcome(s) |
Required Intervention;
|