Brand Name | NUVASIVE GENERAL INSTRUMENTS |
Type of Device | ORTHOPEDIC MANUAL SURGICAL INSTRUMENTS |
Manufacturer (Section D) |
NUVASIVE INC. |
7475 lusk blvd |
san diego CA 92121 |
|
Manufacturer (Section G) |
NUVASIVE INC. |
7475 lusk blvd. |
|
san diego CA 92121 |
|
Manufacturer Contact |
george
panfili
|
7475 lusk blvd |
san diego, CA 92121
|
|
MDR Report Key | 10396692 |
MDR Text Key | 202563490 |
Report Number | 2031966-2020-00160 |
Device Sequence Number | 1 |
Product Code |
LXH
|
UDI-Device Identifier | 00887517390196 |
UDI-Public | 887517390196 |
Combination Product (y/n) | N |
Reporter Country Code | JA |
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 |
08/12/2020 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 08/12/2020 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Health Professional
|
Device Model Number | 6910220 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Was the Report Sent to FDA? |
No
|
Date Manufacturer Received | 07/16/2020 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Reuse
|
Patient Sequence Number | 1 |
Patient Outcome(s) |
Other;
Required Intervention;
|