| Brand Name | ACCUSHAPE PEEK |
| Common Device Name | PEEK CRANIAL IMPLANT |
| Manufacturer (Section D) |
| MEDCAD |
| 501 s 2nd ave. |
| suite a-1000 |
| dallas TX 75226 |
|
| Manufacturer (Section G) |
| MEDCAD |
| 3401 technology dr. |
| unit 3 |
| plano TX 75074 |
|
| Manufacturer Contact |
|
vishvani
patel
|
| 501 s 2nd ave. |
| suite a-1000 |
| dallas, TX 75226
|
|
2144538864
|
|
| MDR Report Key | 22741739 |
| Report Number | 3009196021-2025-00011 |
| Device Sequence Number | 5659490 |
| Product Code |
GXN
|
| UDI-Device Identifier | 00810007630632 |
| UDI-Public | (01)00810007630632(10)251197BOR |
| Combination Product (Y/N) | N |
| Initial Reporter State | TX |
| Initial Reporter Country | US |
| PMA/510(K) Number | K110684 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Device Implanted Year | 2025 |
| Serviced by Third Party (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
Company Representative |
| Initial Reporter Occupation |
Non-Healthcare Professional
|
| Remedial Action |
Replace |
| Type of Report
| Initial |
| Report Date (Section B) |
08/07/2025 |
| 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 Model Number | ZB-SPK40 |
| Device Catalogue Number | ZB-SPK40 |
| Device Lot Number | 251197BOR |
| Was Device Available for Evaluation? |
No
|
| Type of Report(Section G) | Thirty-Day |
| Initial Date Received by Manufacturer | Not provided |
| Initial Report FDA Received Date | 08/07/2025 |
| Was Device Evaluated by Manufacturer? (Y/N) |
No
|
| Date Device Manufactured | 03/14/2025 |
| Is the Device Labeled for Single Use? (Y/N) |
Yes
|
Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N) |
No
|
| Usage of Device |
Initial
|
| Patient Sequence Number | 1 |
| Patient Age | 46 YR |
| Patient Sex | Female |
| Patient Weight | 54 KG |