Device recall
Z-0963-2009: NFix II System 150 mm, Catalog number NX60150-1 spinal fusion surgery
FDA device recall · Class II · Synthes Spine
Key facts
| Recall number (Z-number) | Z-0963-2009 |
|---|---|
| Recall event | 50677 |
| Product | NFix II System 150 mm, Catalog number NX60150-1 spinal fusion surgery |
| Product code | NQP |
| Recalling firm | Synthes Spine |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 5, 2009 |
| 510(k) numbers | K061774 |
| FEI number | 3005180112 |
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