Device recall
Z-2100-2018: VGI MEDICAL VerteLP LATERAL INTERBODY FUSION instrument kit
FDA device recall · Class II · VGI Medical, LLC
Key facts
| Recall number (Z-number) | Z-2100-2018 |
|---|---|
| Recall event | 80012 |
| Product | VGI MEDICAL VerteLP LATERAL INTERBODY FUSION instrument kit |
| Product code | OVD |
| Recalling firm | VGI Medical, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 21, 2020 |
| 510(k) numbers | K151312 |
| FEI number | 3006982954 |
At a glance
- 1–9 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