Device recall
Z-0008-2012: OSTEOMED SPINE Facet Fixation System PrimaLOK FF Threaded Implant Driver Shaft…
FDA device recall · Class II · Osteomed, Lp
Key facts
| Recall number (Z-number) | Z-0008-2012 |
|---|---|
| Recall event | 59213 |
| Product | OSTEOMED SPINE Facet Fixation System PrimaLOK FF Threaded Implant Driver Shaft OsteoMed L.P. 3885 Arapaho Road, Addison, Texas 75001 |
| Product code | MRW |
| Recalling firm | Osteomed, Lp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 4, 2012 |
| 510(k) numbers | K102438 |
| FEI number | 2027754 |
At a glance
- 1–9 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