| Brand Name | FAST-FIX 360 CURVED NDL DELIVERY SYS |
| Common Device Name | SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE |
| Manufacturer (Section D) |
| SMITH & NEPHEW, INC. |
| 130 forbes blvd. |
| mansfield MA 02048 |
|
| Manufacturer (Section G) |
| SMITH & NEPHEW, INC. |
| 130 forbes blvd. |
|
| mansfield MA 02048 |
|
| Manufacturer Contact |
|
holly
topping
|
| 1450 brooks rd. |
| memphis, TN 38116
|
|
5123913905
|
|
| MDR Report Key | 25821109 |
| Report Number | 1219602-2026-02176 |
| Device Sequence Number | 13215111 |
| Product Code |
GAT
|
| UDI-Device Identifier | 00885554023077 |
| UDI-Public | 885554023077 |
| Combination Product (Y/N) | N |
| Initial Reporter Country | CH |
| PMA/510(K) Number | K121861 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Serviced by Third Party (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
Other,Foreign,Health Professional,Company Representative |
| Initial Reporter Occupation |
Physician
|
| Type of Report
| Initial |
| Report Date (Section B) |
07/14/2026 |
| 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
|
| Operator of Device |
Health Professional
|
| Device Catalogue Number | 72202468 |
| Device Lot Number | 2147955 |
| Was Device Available for Evaluation? |
No
|
| Is the Reporter a Health Professional? |
Yes
|
| Type of Report(Section G) | Thirty-Day |
| Initial Date Received by Manufacturer | 06/22/2026 |
| Initial Report FDA Received Date | 07/14/2026 |
| Date Device Manufactured | 03/14/2024 |
| 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 | Unknown |
|
|