Device recall
Z-1900-2020: Cortoss Bone Augmentation Material, Catalog Nos. 2101-0005 and 2101-0010
FDA device recall · Class II · Howmedica Osteonics Corp.
Key facts
| Recall number (Z-number) | Z-1900-2020 |
|---|---|
| Recall event | 85400 |
| Product | Cortoss Bone Augmentation Material, Catalog Nos. 2101-0005 and 2101-0010 |
| Product code | NDN |
| Recalling firm | Howmedica Osteonics Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 27, 2020 |
| 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