Device recall
Z-2103-2013: SpineNet Anterior Cervical Cage, Lordotic, Peek (originally submitted as Daytona…
FDA device recall · Class II · SpineNet
Key facts
| Recall number (Z-number) | Z-2103-2013 |
|---|---|
| Recall event | 65917 |
| Product | SpineNet Anterior Cervical Cage, Lordotic, Peek (originally submitted as Daytona Anterior Cervical Cage) Product Usage: Is indicated for use in skeletally mature patients with degenerative disc disease of the cervical spine with accompanying radicular symptoms at one disc level |
| Product code | ODP |
| Recalling firm | SpineNet |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 2, 2014 |
| 510(k) numbers | K110733 |
| FEI number | 3006755626 |
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