| Brand Name | HUMELOCK REVERSED |
| Common Device Name | REVERSED SHOULDER PROSTHESIS |
| Manufacturer (Section D) |
| FX SOLUTIONS |
| 1663 rue de majornas |
| viriat, 01440 |
| FR 01440 |
|
| MDR Report Key | 11371146 |
| Report Number | 3009532798-2021-00022 |
| Device Sequence Number | 14396236 |
| Product Code |
PHX
|
| UDI-Device Identifier | 03701037300121 |
| UDI-Public | 03701037300121 |
| Combination Product (Y/N) | N |
| Initial Reporter Country | FR |
| PMA/510(K) Number | K150488 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Device Implanted Year | 2019 |
| Device Explanted Year | 2021 |
| Serviced by Third Party (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
company representative,other |
| Initial Reporter Occupation |
Non-Healthcare Professional
|
| Type of Report
| Initial |
| Report Date (Section B) |
02/23/2021 |
| 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
|
| Operator of Device |
Health Professional
|
| Device Expiration Date | 05/01/2024 |
| Device Model Number | DIAMETER 40+3 |
| Device Catalogue Number | 104-0803 |
| Device Lot Number | L2810 |
| Was Device Available for Evaluation? |
No
|
| Type of Report(Section G) | Initial |
| Initial Date Received by Manufacturer | 01/29/2021 |
| Initial Report FDA Received Date | 02/24/2021 |
Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N) |
No
|
| Patient Sequence Number | 1 |
| Outcome Attributed to Adverse Event |
Hospitalization;
Required Intervention;
|
|
|