Device recall
Z-0123-2010: Stryker Instruments Navigation System II PC SPC-1 Assembly, Stryker Navigation…
FDA device recall · Class I · Stryker Instruments Div. of Stryker Corporation
Key facts
| Recall number (Z-number) | Z-0123-2010 |
|---|---|
| Recall event | 53614 |
| Product | Stryker Instruments Navigation System II PC SPC-1 Assembly, Stryker Navigation, Kalamazoo, MI; REF 7700-101-201. The Stryker Navigation System II is a computer-aided surgery platform, supporting surgeons to perform surgical interventions. |
| Product code | HAW |
| Recalling firm | Stryker Instruments Div. of Stryker Corporation |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Dec 31, 2009 |
| 510(k) numbers | K993239 |
| FEI number | 1811755 |
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