Device recall
Z-0967-2009: NFlex Stabilization System 200 mm, Catalog number NF60020-1. spinal fusion…
FDA device recall · Class II · Synthes Spine
Key facts
| Recall number (Z-number) | Z-0967-2009 |
|---|---|
| Recall event | 50677 |
| Product | NFlex Stabilization System 200 mm, Catalog number NF60020-1. spinal fusion surgery |
| Product code | NPQ |
| Recalling firm | Synthes Spine |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 5, 2009 |
| 510(k) numbers | K072685 |
| 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