510(k) K202495 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SIRION Lateral Lumbar Interbody Fusion
| Applicant | Astura Medical, LLC, Irving TX, US |
| Decision | Substantially Equivalent, Jan 6, 2021 |
| Received | Aug 31, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202495
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.