Device recall
Z-0092-2019: AVS Aria Cage, Catalog Number 48753212 Product Usage: The Stryker Spine AVS ARIA…
FDA device recall · Class II · Stryker Spine
Key facts
| Recall number (Z-number) | Z-0092-2019 |
|---|---|
| Recall event | 80971 |
| Product | AVS Aria Cage, Catalog Number 48753212 Product Usage: The Stryker Spine AVS ARIA 1M PEEK Spacers are intervertebral body fusion devices indicated for use with autogenous bone graft in patients with degenerative disc disease (DDD) at one level or two contiguous levels from L2 to S1 . The AVS ARIA TM… |
| Product code | MAX |
| Recalling firm | Stryker Spine |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 23, 2019 |
| 510(k) numbers | K151726 |
| FEI number | 3007331558 |
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