Device recall
Z-0436-2010: Stryker Thor Anterior Plating System; Non Sterile Thor Standard Long Screw 6.0 x…
FDA device recall · Class II · Stryker Spine
Key facts
| Recall number (Z-number) | Z-0436-2010 |
|---|---|
| Recall event | 53606 |
| Product | Stryker Thor Anterior Plating System; Non Sterile Thor Standard Long Screw 6.0 x 61MM, spinal implant component |
| Product code | KWQ |
| Recalling firm | Stryker Spine |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 23, 2013 |
| 510(k) numbers | K073437 |
| FEI number | 3004024955 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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