Brand Name | ZYGAFIX SPINAL FACET SCREW SYSTEM |
Type of Device | SYSTEM, FACET SCREW SPINAL DEVICE |
Manufacturer (Section D) |
XTANT MEDICAL HOLDINGS, INC. |
664 cruiser lane |
belgrade MT 59714 |
|
Manufacturer (Section G) |
XTANT MEDICAL HOLDINGS, INC. |
664 cruiser lane |
|
belgrade MT 59714 |
|
Manufacturer Contact |
rebecca
lennemann
|
664 cruiser lane |
belgrade, MT 59714
|
|
MDR Report Key | 17750290 |
MDR Text Key | 323509764 |
Report Number | 3005031160-2023-00016 |
Device Sequence Number | 1 |
Product Code |
MRW
|
UDI-Device Identifier | M697X07600201 |
UDI-Public | M697X07600201 |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K123932 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Health Professional,User Facility |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial |
Report Date |
09/14/2023 |
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 Model Number | X076-0020 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
08/16/2023
|
Initial Date FDA Received | 09/14/2023 |
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) |
Other;
|
Patient Age | 77 YR |
Patient Sex | Female |
Patient Weight | 59 KG |