Brand Name | FORTIFY |
Type of Device | FORTIFY CORE |
Manufacturer (Section D) |
GLOBUS MEDICAL, INC. |
2560 general armistead avenue |
audubon PA 19403 |
|
Manufacturer (Section G) |
GLOBUS MEDICAL, INC. |
2560 general armistead avenue |
|
audubon PA 19403 |
|
Manufacturer Contact |
daniel
paul
|
2560 general armistead avenue |
audubon, PA 19403
|
6109301800
|
|
MDR Report Key | 14491985 |
MDR Text Key | 300350232 |
Report Number | 3004142400-2022-00085 |
Device Sequence Number | 1 |
Product Code |
MQP
|
Combination Product (y/n) | N |
Reporter Country Code | US |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Company Representative |
Reporter Occupation |
Non-Healthcare Professional
|
Type of Report
| Initial |
Report Date |
05/23/2022 |
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
|
Initial Date Manufacturer Received |
05/09/2022 |
Initial Date FDA Received | 05/24/2022 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
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) |
Other;
|
|
|