Brand Name | NUVASIVE RELINE SYSTEM |
Type of Device | THORACOLUMBOSACRAL PEDICLE SCREW SYSTEM |
Manufacturer (Section D) |
NUVASIVE |
7475 lusk boulevard |
san diego CA 92121 |
|
Manufacturer (Section G) |
NUVASIVE |
7475 lusk boulevard |
|
san diego CA 92121 |
|
Manufacturer Contact |
yobana
sanchez
|
7475 lusk boulevard |
san diego 92121
|
8589093383
|
|
MDR Report Key | 9438691 |
MDR Text Key | 183098421 |
Report Number | 2031966-2019-00261 |
Device Sequence Number | 1 |
Product Code |
NKB
|
Combination Product (y/n) | N |
Reporter Country Code | UK |
PMA/PMN Number | K190636 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
company representative,foreig |
Reporter Occupation |
Physician
|
Type of Report
| Initial |
Report Date |
11/11/2019 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Was the Report Sent to FDA? |
No
|
Initial Date Manufacturer Received |
11/11/2019 |
Initial Date FDA Received | 12/09/2019 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Type of Device Usage |
N
|
Patient Sequence Number | 1 |