Device recall
Z-0275-2016: GMK Hinge knee prosthesis; Model Number: 02.09.TA410; Orthopedics and Orthopedic…
FDA device recall · Class II · Medacta Usa
Key facts
| Recall number (Z-number) | Z-0275-2016 |
|---|---|
| Recall event | 71121 |
| Product | GMK Hinge knee prosthesis; Model Number: 02.09.TA410; Orthopedics and Orthopedic Surgery |
| Product code | KRO |
| Recalling firm | Medacta Usa |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 5, 2017 |
| 510(k) numbers | K130299 |
| FEI number | 3015500078 |
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