Device recall
Z-0211-04: C-Tek Anterior Cervical Plate System: 2.3mm/4.0mm Step Drill-14mm & 2.3mm/4.0mm…
FDA device recall · Class II · Interpore Cross International Inc
Key facts
| Recall number (Z-number) | Z-0211-04 |
|---|---|
| Recall event | 27724 |
| Product | C-Tek Anterior Cervical Plate System: 2.3mm/4.0mm Step Drill-14mm & 2.3mm/4.0mm Step Drill-16mm |
| Product code | DKA |
| Recalling firm | Interpore Cross International Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 20, 2004 |
| FEI number | 1000160576 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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