Device recall
Z-0932-2013: Cynch Lordotic T-PLlF Implant. Intervertebral fusion device with bone graft, for…
FDA device recall · Class II · Spine Smith Partners LP
Key facts
| Recall number (Z-number) | Z-0932-2013 |
|---|---|
| Recall event | 62993 |
| Product | Cynch Lordotic T-PLlF Implant. Intervertebral fusion device with bone graft, for use with supplemental fixation. |
| Product code | MAX |
| Recalling firm | Spine Smith Partners LP |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 17, 2013 |
| 510(k) numbers | K101085 |
| FEI number | 3010266937 |
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