Device recall
Z-1019-2016: Virage OCT Spinal Fixation System. Intended to promote fusion of the…
FDA device recall · Class II · Zimmer Spine, Inc.
Key facts
| Recall number (Z-number) | Z-1019-2016 |
|---|---|
| Recall event | 73265 |
| Product | Virage OCT Spinal Fixation System. Intended to promote fusion of the Occipital-Cervical-Thoracic spine (Occiput-T3). |
| Product code | KWP |
| Recalling firm | Zimmer Spine, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 11, 2016 |
| 510(k) numbers | K133556 |
| FEI number | 1000115775 |
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