Device recall
Z-0952-2017: SCREW 02.7-12MM LOCKING, REF W27 ST112: a) DRP, b) NEO, In2Bones, 28 chemin du…
FDA device recall · Class II · In2Bones, SAS
Key facts
| Recall number (Z-number) | Z-0952-2017 |
|---|---|
| Recall event | 76104 |
| Product | SCREW 02.7-12MM LOCKING, REF W27 ST112: a) DRP, b) NEO, In2Bones, 28 chemin du petit bois, 69130 Ecully - France The NEOVIEW Plating System is intended for fixation of intra-articular and extraarticular fractures of the distal radius and reconstruction of the distal radius |
| Product code | HRS |
| Recalling firm | In2Bones, SAS |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 1, 2017 |
| 510(k) numbers | K160995 |
| FEI number | 3010470577 |
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