Brand Name | DONJOY TITANIUM, A22 |
Type of Device | JOINT, KNEE, EXTERNAL BRACE |
Manufacturer (Section D) |
DJO, LLC |
1430 decision street |
vista CA 92081 9663 |
|
Manufacturer (Section G) |
DJO, LLC |
3151 scott st. |
|
vista CA 92081 9663 |
|
Manufacturer Contact |
brian
becker
|
2900 lake vista drive |
lewisville, TX 75067
|
|
MDR Report Key | 8822998 |
MDR Text Key | 152086931 |
Report Number | 3012446970-2019-00024 |
Device Sequence Number | 1 |
Product Code |
ITQ
|
Combination Product (y/n) | N |
PMA/PMN Number | EXEMPT |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
consumer |
Type of Report
| Initial |
Report Date |
07/24/2019 |
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? |
No
|
Device Operator |
Lay User/Patient
|
Device Model Number | CONV TITANIUM |
Was Device Available for Evaluation? |
No
|
Initial Date Manufacturer Received |
07/01/2019
|
Initial Date FDA Received | 07/24/2019 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 01/09/2018 |
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Unknown
|
Patient Sequence Number | 1 |
Patient Outcome(s) |
Required Intervention;
|
|
|