Device recall
Z-0069-2021: NUVASIVE SPECIALIZED ORTHOPEDICS, INC. Precice Bone Transport Antegrade Femur…
FDA device recall · Class II · Nuvasive Specialized Orthopedics Inc
Key facts
| Recall number (Z-number) | Z-0069-2021 |
|---|---|
| Recall event | 86150 |
| Product | NUVASIVE SPECIALIZED ORTHOPEDICS, INC. Precice Bone Transport Antegrade Femur Trochanter 10 Degree Bend Component of the orthopedic Precice Bone Transport System of intramedullary nail, locking screws, reusable instruments, and hand-held External Remote Controller (ERC). |
| Product code | HSB |
| Recalling firm | Nuvasive Specialized Orthopedics Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K193016, K201567 |
| FEI number | 3006179046 |
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