Brand Name | TIBIAL INSERT, FB, SZ 3, RT, 7MM |
Type of Device | TIBIAL INSERT |
Manufacturer (Section D) |
EXACTECH, INC. |
2320 nw 66th ct |
gainesville FL 32653 |
|
MDR Report Key | 6672606 |
MDR Text Key | 78546460 |
Report Number | 1038671-2017-00420 |
Device Sequence Number | 1 |
Product Code |
HSN
|
Combination Product (y/n) | N |
PMA/PMN Number | K152217 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
company representative,health |
Type of Report
| Initial,Followup |
Report Date |
01/14/2019 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 06/28/2017 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Physician
|
Device Catalogue Number | 350-22-13 |
Was Device Available for Evaluation? |
No
|
Date Manufacturer Received | 01/14/2019 |
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Patient Sequence Number | 1 |
Patient Outcome(s) |
Required Intervention;
|
|
|