Device recall
Z-1127-2013: The Oxford Partial Knee; Oxford Knee Resection Procedure 3 Pack CEMENTED For use…
FDA device recall · Class II · Synvasive Technology Inc
Key facts
| Recall number (Z-number) | Z-1127-2013 |
|---|---|
| Recall event | 64646 |
| Product | The Oxford Partial Knee; Oxford Knee Resection Procedure 3 Pack CEMENTED For use with Stryker System 5, System 4, System 2000 and EDH. Product Usage: For use with Stryker System 5, System 4, System 2000 and EDH. A set of three surgical saw blades is used to resect damaged cartilage and/or bone in an… |
| Product code | HSD |
| Recalling firm | Synvasive Technology Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 13, 2014 |
| 510(k) numbers | K911902 |
| FEI number | 1000123893 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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