510(k) K242509 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
HAnano InterFuse(R) Modular Interbody
| Applicant | Next Orthosurgical, Vista CA, US |
| Decision | Substantially Equivalent, Sep 19, 2024 |
| Received | Aug 22, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K242509
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.