Device recall
Z-0047-2012: PERPOS Driver; Catalog # 6112 Interventional Spine, Inc. A cannulated, driver to…
FDA device recall · Class II · Interventional Spine Inc
Key facts
| Recall number (Z-number) | Z-0047-2012 |
|---|---|
| Recall event | 58461 |
| Product | PERPOS Driver; Catalog # 6112 Interventional Spine, Inc. A cannulated, driver to be used over a K-wire to engage the head of the 4.5mm BONE-LOK PLS Implant (LSW-45-3040) and drive it into the bone. The PERPOS Driver (61 12) is sold as either a component of the Single Use PERPOS PLS System (9045-01… |
| Product code | HXX |
| Recalling firm | Interventional Spine Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 5, 2013 |
| FEI number | 3003523239 |
At a glance
- None 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