Device recall
Z-0977-2015: lnline Persuader- PedFuse Pedicle Screw System; Part Number: 11-80164
FDA device recall · Class II · SpineFrontier, Inc.
Key facts
| Recall number (Z-number) | Z-0977-2015 |
|---|---|
| Recall event | 70065 |
| Product | lnline Persuader- PedFuse Pedicle Screw System; Part Number: 11-80164 |
| Product code | LXH |
| Recalling firm | SpineFrontier, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 11, 2016 |
| FEI number | 3005977257 |
At a glance
- None 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