Device recall
Z-0677-05: Fill Tube,diverted, Catalog # 300-1002, is used for the delivery of granular…
FDA device recall · Class III · The Spineology Group
Key facts
| Recall number (Z-number) | Z-0677-05 |
|---|---|
| Recall event | 31198 |
| Product | Fill Tube,diverted, Catalog # 300-1002, is used for the delivery of granular autograft or allograft into Spineology''s OptiMesh implant. Fill tube is identified with Spineology, catalog number and lot number printed directly onto the metal. |
| Product code | LXH |
| Recalling firm | The Spineology Group |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 17, 2005 |
| 510(k) numbers | K014200 |
| FEI number | 3003179719 |
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