Brand Name | FMP HIP |
Type of Device | FMP HEMISPHERICAL SHELLS W/SCREW HOLES, 54MM, W/P2 COATING |
Manufacturer (Section D) |
ENCORE MEDICAL, L.P. |
9800 metric blvd. |
austin TX 78758 |
|
Manufacturer (Section G) |
ENCORE MEDICAL, L.P. |
9800 metric blvd. |
|
austin TX 78758 |
|
Manufacturer Contact |
teffany
hutto
|
9800 metric blvd. |
austin, TX 78758-5445
|
5128346255
|
|
MDR Report Key | 3934530 |
MDR Text Key | 16186343 |
Report Number | 1644408-2014-00449 |
Device Sequence Number | 1 |
Product Code |
LPH
|
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K974093 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Company Representative |
Reporter Occupation |
Other
|
Type of Report
| Initial,Followup |
Report Date |
07/10/2014 |
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 |
Health Professional
|
Device Expiration Date | 04/30/2020 |
Device Catalogue Number | 430-98-054 |
Device Lot Number | 590G1033 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
No
|
Initial Date Manufacturer Received |
02/12/2015
|
Initial Date FDA Received | 07/15/2014 |
Supplement Dates Manufacturer Received | Not provided
|
Supplement Dates FDA Received | 03/02/2015
|
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 04/23/2014 |
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 |
Treatment | (B)(4), LOT 692F1097; (B)(4), LOT 866B1056 |
Patient Outcome(s) |
Required Intervention;
|
Patient Age | 70 YR |
|
|