Device recall
Z-1023-2017: Medacta International SA, M.U.S.T. Rod, REF 03.50.433, Size 5.5mm, Length 480mm…
FDA device recall · Class II · Medacta Usa Inc
Key facts
| Recall number (Z-number) | Z-1023-2017 |
|---|---|
| Recall event | 76034 |
| Product | Medacta International SA, M.U.S.T. Rod, REF 03.50.433, Size 5.5mm, Length 480mm, Type Straight, Mat Co-Cr-Mo The rods act as a connector between the different pedicle screws to create a stable construct for the stabilization and fusion of the lumbar and thoracic spine. Indications for Use: The… |
| Product code | KWP |
| Recalling firm | Medacta Usa Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 15, 2017 |
| 510(k) numbers | K121115 |
| FEI number | 3006639916 |
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