Brand Name | ATTUNE CR FB INSRT SZ 8 6MM |
Type of Device | KNEE TIBIAL BEARING/INSERT |
Manufacturer (Section D) |
DEPUY ORTHOPAEDICS, INC. |
700 orthopaedic drive |
warsaw IN 46582 |
|
Manufacturer (Section G) |
DEPUY ORTHOPAEDICS, INC. |
700 orthopaedic drive |
|
warsaw IN 46582 |
|
Manufacturer Contact |
stacey
trick
|
700 orthopaedic drive |
warsaw, IN 46581
|
5743714554
|
|
MDR Report Key | 3891981 |
MDR Text Key | 4653014 |
Report Number | 1818910-2014-21823 |
Device Sequence Number | 1 |
Product Code |
JWH
|
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | PK101433 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Foreign,Health Professional |
Reporter Occupation |
Physician
|
Type of Report
| Initial,Followup |
Report Date |
06/05/2014 |
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 |
Physician
|
Device Catalogue Number | 151620806 |
Device Lot Number | 220880 |
Was Device Available for Evaluation? |
Device Returned to Manufacturer
|
Date Returned to Manufacturer | 06/11/2014 |
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
09/04/2014 |
Initial Date FDA Received | 06/24/2014 |
Supplement Dates Manufacturer Received | Not provided
|
Supplement Dates FDA Received | 09/04/2014
|
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) |
Required Intervention;
|
Patient Age | 69 YR |