Device recall
Z-1989-2015: Nakoma-SL Anterior Cervical Plating System's Variable Single Barrel Drill Guide…
FDA device recall · Class II · Alliance Partners LLC
Key facts
| Recall number (Z-number) | Z-1989-2015 |
|---|---|
| Recall event | 71457 |
| Product | Nakoma-SL Anterior Cervical Plating System's Variable Single Barrel Drill Guide Product Usage: The Nakoma-SL ACP System is intended for anterior intervertebral screw fixation of the cervical spine at levels C2-T1. The Nakoma ACP System is indicated for temporary stabilization of the anterior spine… |
| Product code | KWQ |
| Recalling firm | Alliance Partners LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 9, 2015 |
| 510(k) numbers | K141993 |
| FEI number | 3008520015 |
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