510(k) K151726 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
AVS AL and AVS ALign PEEK Spacers, AVS PL and AVS UniLIF PEEK Spacers, AVS TL PEEK Spacer, AVS Navigator PEEK Spacer, AVS ARIA PEEK Spacer
| Applicant | Stryker Corporation, Allendale NJ, US |
| Decision | Substantially Equivalent, Jan 20, 2016 |
| Received | Jun 26, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151726
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 13, 2018 | Stryker Spine 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 d Terminated |
MAX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.