Brand Name | NUVECTRA CORPORATION |
Type of Device | STIMULATOR, SPINAL CORD, TOTALLY IMPLANTABLE (PAIN RELIEF) |
Manufacturer (Section D) |
NUVECTRA CORPORATION |
10675 naples street ne |
blaine MN 55449 |
|
Manufacturer (Section G) |
NUVECTRA CORPORATION |
10675 naples street ne |
|
blaine MN 55449 |
|
Manufacturer Contact |
david
douglas
|
10675 naples street ne |
blaine, MN 55449
|
7634047531
|
|
MDR Report Key | 8753155 |
MDR Text Key | 150120564 |
Report Number | 3010309840-2019-00219 |
Device Sequence Number | 1 |
Product Code |
LGW
|
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | P130028 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
company representative,health |
Reporter Occupation |
Physician
|
Type of Report
| Initial |
Report Date |
07/02/2019 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 07/02/2019 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Expiration Date | 06/04/2020 |
Device Model Number | 1124-60 |
Device Catalogue Number | 1124-60 |
Device Lot Number | W4348023 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Date Manufacturer Received | 06/03/2019 |
Was Device Evaluated by Manufacturer? |
No
|
Date Device Manufactured | 06/04/2018 |
Is the Device Single Use? |
Yes
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
N
|
Patient Sequence Number | 1 |
Patient Outcome(s) |
Required Intervention;
|
Patient Age | 47 YR |
|
|