Brand Name | CTI KNEE BRACE |
Type of Device | ORTHOSIS, LIMB BRACE |
Manufacturer (Section D) |
OSSUR |
blvd hector teran teran 2102 |
edificio #1, col. de canon del |
tijuana, baja california 2102 |
MX 2102 |
|
Manufacturer (Section G) |
OSSUR |
27051 towne centre |
|
foothill ranch CA 92610 |
|
Manufacturer Contact |
karen
montes
|
27051 towne centre |
foothill ranch, CA 92610
|
9493823741
|
|
MDR Report Key | 4961206 |
MDR Text Key | 6190680 |
Report Number | 3008523132-2015-00002 |
Device Sequence Number | 1 |
Product Code |
IQI
|
Combination Product (y/n) | N |
Reporter Country Code | US |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Consumer,consumer |
Reporter Occupation |
Patient
|
Type of Report
| Initial |
Report Date |
09/30/2015 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 07/28/2015 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Lay User/Patient
|
Device Model Number | B-7095000025 |
Device Catalogue Number | B-7095000025 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
No
|
Date Manufacturer Received | 07/10/2015 |
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) |
Required Intervention;
|
|
|