510(k) K223335 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SIRION Lateral Lumbar Interbody System
| Applicant | Astura Medical, Irving TX, US |
| Decision | Substantially Equivalent, May 9, 2023 |
| Received | Nov 1, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223335
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.