Device recall
Z-1697-2021: Cascadia AN Interbody Convex 10x28x14mm Catalog Number: 6101-2102814NC-G2 Lumbar…
FDA device recall · Class II · K2M, Inc
Key facts
| Recall number (Z-number) | Z-1697-2021 |
|---|---|
| Recall event | 87905 |
| Product | Cascadia AN Interbody Convex 10x28x14mm Catalog Number: 6101-2102814NC-G2 Lumbar implants are intervertebral body fusion devices indicated for use with autograft and/or allogenic bone graft comprised of cancellous and/or corticocancellous bone graft when used as anadjunct to fusion in patients with… |
| Product code | MAX |
| Recalling firm | K2M, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 8, 2023 |
| 510(k) numbers | K150481, K172009 |
| FEI number | 3008599177 |
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