Device recall
Z-1691-2017: Altius M-INI OCT Posterior Spinal Fixation System, Model Number 1200-9216 The…
FDA device recall · Class II · Zimmer Biomet Spine, Inc
Key facts
| Recall number (Z-number) | Z-1691-2017 |
|---|---|
| Recall event | 76610 |
| Product | Altius M-INI OCT Posterior Spinal Fixation System, Model Number 1200-9216 The AltiusTM OCT and AltiusTM M-INITM OCT Systems when intended to promote fusion of the cervical spine and occipitocervico-thoracic junction (Occiput-T3), these systems are indicated for: DDD (neck pain of discogenic origin… |
| Product code | MAX |
| Recalling firm | Zimmer Biomet Spine, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 30, 2018 |
| FEI number | 3012447612 |
At a glance
- None 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