Device recall
Z-1461-2017: L-Varlock Cage/Trial Implant Holder, Reference HD0060, Kisco International…
FDA device recall · Class II · Kiscomedica S.A.
Key facts
| Recall number (Z-number) | Z-1461-2017 |
|---|---|
| Recall event | 76494 |
| Product | L-Varlock Cage/Trial Implant Holder, Reference HD0060, Kisco International, France. Product Usage: The L-Varlock Lumbar Cage is indicated for intervertebral body fusion procedures in skeletally mature patients with degenerative disc disease (DDD) of the lumbar spine at one or two contiguous levels… |
| Product code | MAX |
| Recalling firm | Kiscomedica S.A. |
| Recall class | Class II |
| Status | Terminated |
| 510(k) numbers | K080537 |
| FEI number | 3005440746 |
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