Device recall
Z-3210-2024: AVS Anchor-C Cervical Cage System Instructions For Use (IFU)- eIFU (revision…
FDA device recall · Class II · Stryker Spine
Key facts
| Recall number (Z-number) | Z-3210-2024 |
|---|---|
| Recall event | 95274 |
| Product | AVS Anchor-C Cervical Cage System Instructions For Use (IFU)- eIFU (revision 5)-Indicated for anterior cervical interbody fusion procedures in skeletally mature patients with cervical disc disease at one level from the C2-C3 disc to the C7-T1 disc. |
| Product code | OVE |
| Recalling firm | Stryker Spine |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K102606 |
| FEI number | 3004024955 |
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