Device recall
Z-1258-06: St. Francis Medical Technologies brand X STOP Interspinous Process Decompression…
FDA device recall · Class II · St. Francis Medical Technologies Inc
Key facts
| Recall number (Z-number) | Z-1258-06 |
|---|---|
| Recall event | 35621 |
| Product | St. Francis Medical Technologies brand X STOP Interspinous Process Decompression (IPD) System, 14 mm X STOP implants in peel pouch, Catalog #1-2210; The X STOP consists of a main body, a spacer, and a tissue expander that is secured using a universal wing assembly consisting of a wing and a… |
| Product code | NQO |
| Recalling firm | St. Francis Medical Technologies Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 21, 2006 |
| PMA numbers | P040001 |
| FEI number | 3004904811 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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