Device recall
Z-0292-06: SC-AcuFix Core Instruments Surgical Techniques covering SC-AcuFix SlimLine…
FDA device recall · Class II · Abbott Spine
Key facts
| Recall number (Z-number) | Z-0292-06 |
|---|---|
| Recall event | 34015 |
| Product | SC-AcuFix Core Instruments Surgical Techniques covering SC-AcuFix SlimLine, SlimLine Hybrid, Corpectomy, ThinLine and Ant-Cer Anterior Cervical Plating Systems. |
| Product code | KWQ |
| Recalling firm | Abbott Spine |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 2, 2007 |
| 510(k) numbers | K013979, K024326, K990005 |
| FEI number | 3000718496 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database