Brand Name | IUNI G2 |
Type of Device | UNICONDYLAR KNEE REPLACEMENT SYSTEM |
Manufacturer (Section D) |
CONFORMIS, INC. |
600 technology park drive |
billerica MA 01821 |
|
Manufacturer (Section G) |
CONFORMIS, INC. |
600 research drive |
|
wilmington MA 01887 |
|
Manufacturer Contact |
thomas
haueter
|
600 technology park drive |
billerica, MA 01821
|
7813459161
|
|
MDR Report Key | 8459704 |
MDR Text Key | 140159371 |
Report Number | 3004153240-2019-00080 |
Device Sequence Number | 1 |
Product Code |
HSX
|
UDI-Device Identifier | M5722INT0600210 |
UDI-Public | +M5722INT0600210 |
Combination Product (y/n) | N |
Reporter Country Code | GM |
PMA/PMN Number | K133256 |
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 |
Report Date |
03/28/2019 |
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 |
Health Professional
|
Device Catalogue Number | M5722INT0600210 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
03/18/2019 |
Initial Date FDA Received | 03/28/2019 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 06/25/2016 |
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 | 59 YR |