Device recall
Z-1413-2011: Stryker Navigation System - SpineMap 3D - Planning, Part number 6002-651-000. It…
FDA device recall · Class II · Stryker Instruments Division of Stryker Corporation
Key facts
| Recall number (Z-number) | Z-1413-2011 |
|---|---|
| Recall event | 57487 |
| Product | Stryker Navigation System - SpineMap 3D - Planning, Part number 6002-651-000. It provides precise stereostatic determination of surgical targets using stereostatic methodology. The three principle features include computer calculation of stereostatic coordinates from the diagnostic images… |
| Product code | HAW |
| Recalling firm | Stryker Instruments Division of Stryker Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 1, 2011 |
| 510(k) numbers | K062640 |
| FEI number | 1811755 |
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