Device recall
Z-1455-2012: Quintex Cervical Plating System - Screws. The Quintex Cervical Plating System is…
FDA device recall · Class II · Aesculap Implant Systems
Key facts
| Recall number (Z-number) | Z-1455-2012 |
|---|---|
| Recall event | 61346 |
| Product | Quintex Cervical Plating System - Screws. The Quintex Cervical Plating System is intended for the treatment of cervical spinal instability. The Quintex Cervical Screws are available in three different versions: semi-constrained, constrained, and dynamic. The screws all have a head diameter of 4.0mm… |
| Product code | KWQ |
| Recalling firm | Aesculap Implant Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 13, 2012 |
| 510(k) numbers | K100243 |
| FEI number | 2916714 |
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