Brand Name | EQUINOXE REVERSE 38MM HUMERAL LINER +0 |
Type of Device | PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED |
Manufacturer (Section D) |
EXACTECH, INC. |
2320 nw 66 court |
gainesville FL 32653 |
|
Manufacturer (Section G) |
EXACTECH, INC. |
2320 nw 66th ct |
|
gainesville FL 32653 |
|
Manufacturer Contact |
michael
crader
|
2320 nw 66th ct |
gainesville, FL 32653
|
3523771140
|
|
MDR Report Key | 18892979 |
MDR Text Key | 337515746 |
Report Number | 1038671-2024-00485 |
Device Sequence Number | 1 |
Product Code |
KWT
|
Combination Product (y/n) | N |
Reporter Country Code | AS |
PMA/PMN Number | K063569 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Health Professional,Company Representative |
Reporter Occupation |
Physician
|
Type of Report
| Initial |
Report Date |
03/13/2024 |
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 | 320-38-00 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
02/22/2024
|
Initial Date FDA Received | 03/13/2024 |
Was Device Evaluated by Manufacturer? |
No
|
Date Device Manufactured | 07/31/2023 |
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 | SEE H10 |
Patient Outcome(s) |
Required Intervention;
|
Patient Age | 77 YR |
Patient Sex | Male |
|
|