Device recall
Z-1976-2013: Stryker Oasys Midline Occiput Plate-1) Small 2) Medium 3) Large 4) Large Long 5)…
FDA device recall · Class I · Stryker Spine
Key facts
| Recall number (Z-number) | Z-1976-2013 |
|---|---|
| Recall event | 65777 |
| Product | Stryker Oasys Midline Occiput Plate-1) Small 2) Medium 3) Large 4) Large Long 5) Mini. Allows for positioning directly on the midline keel of the occiput. |
| Product code | KWP |
| Recalling firm | Stryker Spine |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Dec 30, 2014 |
| 510(k) numbers | K093670 |
| FEI number | 3004024955 |
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