Device recall
Z-2335-2010: Abbott Spine PathFinder, Cannulated Poly Screwdriver II - MOD, non-sterile…
FDA device recall · Class II · Zimmer Inc.
Key facts
| Recall number (Z-number) | Z-2335-2010 |
|---|---|
| Recall event | 53811 |
| Product | Abbott Spine PathFinder, Cannulated Poly Screwdriver II - MOD, non-sterile, Manufactured by Abbott Spine, Inc., Austin, TX; Ref. 1160-2. Usage: The screwdriver is intended to mate to the hexalobular feature of a PathFinder open polyaxial screw and threads onto the head to hold it in on-axis for… |
| Product code | MNI |
| Recalling firm | Zimmer Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 22, 2010 |
| 510(k) numbers | K030625 |
| FEI number | 1000220733 |
At a glance
- 1–9 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