Device recall
Z-2101-2021: Cortoss Bone Augmentation Material 10cc Cartridge, Catalog Number 2101-0010…
FDA device recall · Class II · Stryker Spine
Key facts
| Recall number (Z-number) | Z-2101-2021 |
|---|---|
| Recall event | 88217 |
| Product | Cortoss Bone Augmentation Material 10cc Cartridge, Catalog Number 2101-0010, GTIN 00808232000979 |
| Product code | NDN |
| Recalling firm | Stryker Spine |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 15, 2022 |
| 510(k) numbers | K080108 |
| 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