Device recall
Z-0535-2013: Titan Spine Endoskeleton TA Implant products. 2107-0118 18mm Standard…
FDA device recall · Class II · TITAN SPINE, LLC
Key facts
| Recall number (Z-number) | Z-0535-2013 |
|---|---|
| Recall event | 63549 |
| Product | Titan Spine Endoskeleton TA Implant products. 2107-0118 18mm Standard Endoskeleton Implant VBR 2107-0120 20mm Standard Endoskeleton Implant VBR 2107-0218 18mm Large Endoskeleton Implant VBR 2107-0220 20mm Large Endoskeleton Implant VBR Endoskeleton TA VBR is intended for use in the thoracolumbar… |
| Product code | MQP |
| Recalling firm | TITAN SPINE, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 14, 2013 |
| 510(k) numbers | K032812 |
| FEI number | 3006340236 |
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