Device recall
Z-0923-2010: Medtronic Orthopedic Dovetail Clamp, REF 9730289, Medtronic Navigation…
FDA device recall · Class II · Medtronic Navigation, Inc
Key facts
| Recall number (Z-number) | Z-0923-2010 |
|---|---|
| Recall event | 54381 |
| Product | Medtronic Orthopedic Dovetail Clamp, REF 9730289, Medtronic Navigation, Louisville, CO 80027. In combination with a tera-tracker reference frame, is used by an Orthopedic surgeon to navigate the location of an acetabular cup positioner/impactor during hip replacement surgery. |
| Product code | HAW |
| Recalling firm | Medtronic Navigation, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 13, 2010 |
| 510(k) numbers | K021980 |
| FEI number | 1000517638 |
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