510(k) K203531 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
XYPAN Expandable Lumbar Cage System
| Applicant | Aegis Spine, Inc., Englewood CO, US |
| Decision | Substantially Equivalent, Jan 29, 2021 |
| Received | Dec 2, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203531
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.