Device recall
Z-0400-2014: LANX Timberline MPF Lateral Modular Plate Fixation System Straight Split Tip…
FDA device recall · Class II · Lanx, Inc.
Key facts
| Recall number (Z-number) | Z-0400-2014 |
|---|---|
| Recall event | 66836 |
| Product | LANX Timberline MPF Lateral Modular Plate Fixation System Straight Split Tip Driver - Short ("Driver"). Model Number 8630-0107. The Timberline MPF device is an intervertebral body fusion device consisting of a PEEK intervertebral spacer, titanium plate, and screws. The PEEK spacer has a generally… |
| Product code | OVD |
| Recalling firm | Lanx, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 29, 2015 |
| 510(k) numbers | K123767, K131547 |
| FEI number | 3012447612 |
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