Device recall
Z-0290-2017: RTI Surgical Streamline OCT Occipito-Cervico-Thoracic Spinal Rod, CoCr, 3.2mm…
FDA device recall · Class II · RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
Key facts
| Recall number (Z-number) | Z-0290-2017 |
|---|---|
| Recall event | 75242 |
| Product | RTI Surgical Streamline OCT Occipito-Cervico-Thoracic Spinal Rod, CoCr, 3.2mm (D) x 240mm (L) Product Usage: When intended to promote fusion of the cervical spine and occipitocervico-thoracic junction (occiput-T3), the Streamline OCT Occipito-Cervico-Thoracic System is intended for: degenerative… |
| Product code | KWP |
| Recalling firm | RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 1, 2017 |
| 510(k) numbers | K150254 |
| FEI number | 1000115331 |
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