Device recall
Z-0711-05: Stealth Station Cranial Application v.4.5
FDA device recall · Class II · Medtronic Surgical Navigation Technologies, Inc
Key facts
| Recall number (Z-number) | Z-0711-05 |
|---|---|
| Recall event | 31133 |
| Product | Stealth Station Cranial Application v.4.5 |
| Product code | HAW |
| Recalling firm | Medtronic Surgical Navigation Technologies, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 15, 2005 |
| 510(k) numbers | K954276 |
| FEI number | 1000517638 |
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