Device recall
Z-2213-2026: OneLIF Interbody Cage (REF/Description): 010-107-1007/Small 7 Degree 10mm X 7mm…
FDA device recall · Class II · Novapproach Spine, LLC
Key facts
| Recall number (Z-number) | Z-2213-2026 |
|---|---|
| Recall event | 98835 |
| Product | OneLIF Interbody Cage (REF/Description): 010-107-1007/Small 7 Degree 10mm X 7mm, 010-107-1007-2/Small 7 Degree 10mm X 7mm - Oblique, 010-107-1209/Small 7 Degree 12mm X 9mm, 010-107-1411/Small 7 Degree 14mm X 11mm, 010-107-1613/Small 7 Degree 16mm X 13mm, 010-113-1006/Small, 13 Degree 10mm X 6mm… |
| Product code | OVD |
| Recalling firm | Novapproach Spine, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K211769 |
| FEI number | 3020307303 |
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