| Brand Name | Swift-Lock Anchor |
| Common Device Name | SCS ANCHOR |
| Manufacturer (Section D) |
| Abbott Medical |
| 6901 preston rd |
| plano TX 75024 |
|
| Manufacturer (Section G) |
| Abbott Medical |
| 6901 preston rd |
|
| plano TX 75024 |
|
| Manufacturer Contact |
|
sara
speyerer
|
| 6901 preston road |
| plano, TX 75024
|
|
+1(972)309-8000
|
|
| MDR Report Key | 50811517 |
| Report Number | 1627487-2026-10135 |
| Device Sequence Number | 18786984 |
| Product Code |
GZB
|
| UDI-Device Identifier | 05415067024084 |
| UDI-Public | (01)05415067024084(10)7319788(17)220109 |
| Combination Product (Y/N) | N |
| Initial Reporter State | MN |
| Initial Reporter Country | US |
| PMA/510(K) Number | K092371 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Device Implanted Year | 2020 |
| Device Explanted Year | 2026 |
| Serviced by Third Party (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
Health Professional,Company Representative |
| Initial Reporter Occupation |
Physician
|
| Type of Report
| Initial |
| Report Date (Section B) |
09/17/2026 |
| 1 Device was Involved in the Event |
|
| 1 Patient was Involved in the Event |
|
| Operator of Device |
Health Professional
|
| Device Expiration Date | 01/09/2022 |
| Device Model Number | 1192 |
| Device Catalogue Number | 1192 |
| Device Lot Number | 7319788 |
| Was Device Available for Evaluation? |
No
|
| Is the Reporter a Health Professional? |
Yes
|
| Was the Report Sent to FDA? |
No
|
| Type of Report(Section G) | Thirty-Day |
| Initial Date Received by Manufacturer | 08/27/2026 |
| Initial Report FDA Received Date | 09/17/2026 |
| Was Device Evaluated by Manufacturer? (Y/N) |
No
|
| Date Device Manufactured | 01/10/2020 |
| 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 Sex | Female |
| Patient Weight | 140 LB |