Brand Name | AMS ADVANCE XP SLING SYSTEM |
Type of Device | MESH SURGICAL FOR STRESS URINARY INCONTINENCE MALE |
Manufacturer (Section D) |
BOSTON SCIENTIFIC CORPORATION |
300 boston scientific way |
marlborough MA 01752 |
|
Manufacturer (Section G) |
BOSTON SCIENTIFIC CORPORATION |
300 boston scientific way |
|
marlborough MA 01752 |
|
Manufacturer Contact |
farshad
fahimi
|
4100 hamline avenue north |
building c |
saint paul, MN 55112
|
|
MDR Report Key | 19050230 |
MDR Text Key | 339476132 |
Report Number | 2124215-2024-20735 |
Device Sequence Number | 1 |
Product Code |
OTM
|
Combination Product (y/n) | N |
Reporter Country Code | CA |
PMA/PMN Number | K182169 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Other,Foreign,Health Professional |
Reporter Occupation |
Physician
|
Type of Report
| Initial |
Report Date |
04/05/2024 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Lay User/Patient
|
Device Model Number | UNK-P-SLING-MENS_ADVANCE_XP |
Device Catalogue Number | UNK-P-SLING-MENS_ADVANCE_XP |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
04/04/2024 |
Initial Date FDA Received | 04/05/2024 |
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) |
Hospitalization;
Required Intervention;
|
Patient Age | 71 YR |
Patient Sex | Male |