Brand Name | FOOTPRINT ULTRA PK SUTURE ANCHOR, 4.5 |
Type of Device | FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE |
Manufacturer (Section D) |
SMITH & NEPHEW, INC. |
130 forbes boulevard |
mansfield MA 02048 |
|
Manufacturer (Section G) |
SMITH & NEPHEW, INC. |
130 forbes boulevard |
|
mansfield MA 02048 |
|
Manufacturer Contact |
jim
gonzales
|
7000 west william cannon drive |
austin, TX 78735
|
|
MDR Report Key | 7316890 |
MDR Text Key | 101718382 |
Report Number | 1219602-2018-00292 |
Device Sequence Number | 1 |
Product Code |
MBI
|
UDI-Device Identifier | 03596010650528 |
UDI-Public | (01)03596010650528(17)221215(10)50703018 |
Combination Product (y/n) | N |
Reporter Country Code | SF |
PMA/PMN Number | K093897 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
distributor,foreign,health pr |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial,Followup |
Report Date |
04/03/2018 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Expiration Date | 12/15/2022 |
Device Model Number | 72202901 |
Device Catalogue Number | 72202901 |
Device Lot Number | 50703018 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
02/08/2018 |
Initial Date FDA Received | 03/06/2018 |
Supplement Dates Manufacturer Received | 03/26/2018
|
Supplement Dates FDA Received | 04/03/2018
|
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 12/15/2017 |
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 Age | 64 YR |