Device recall
Z-1897-2026: nanOss 3D Advanced Bone Graft Substitute nanOss 3D Plus Advanced Bone Graft…
FDA device recall · Class II · XTANT Medical Holdings, Inc
Key facts
| Recall number (Z-number) | Z-1897-2026 |
|---|---|
| Recall event | 98643 |
| Product | nanOss 3D Advanced Bone Graft Substitute nanOss 3D Plus Advanced Bone Graft Substitute 90-300-251008: nanOss 3D Advanced Bone Graft Substitute, 25x100x8mm, 20cc 90-300-25508: nanOss 3D Advanced Bone Graft Substitute, 25x50x8mm, 10cc 90-300-251004: nanOss 3D Advanced Bone Graft Substitute… |
| Product code | MQV |
| Recalling firm | XTANT Medical Holdings, Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K132050 |
| FEI number | 3005031160 |
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