Device recall
Z-0627-2014: C-Plus" 10mm x 12mm Webless implants Pioneer Surgical's C-Plus " 10mm x 12mm…
FDA device recall · Class II · RTI Surgical, Inc.
Key facts
| Recall number (Z-number) | Z-0627-2014 |
|---|---|
| Recall event | 67093 |
| Product | C-Plus" 10mm x 12mm Webless implants Pioneer Surgical's C-Plus " 10mm x 12mm Webless implants are cervical intervertebral fusion devices that are intended to stabilize a cervical spinal segment to promote fusion in order to restrict motion and decrease pain. They are intended for use with… |
| Product code | ODP |
| Recalling firm | RTI Surgical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 26, 2014 |
| 510(k) numbers | K073177 |
| FEI number | 1000115331 |
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