510(k) K231241 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
NanoHive Medical Lumbar Interbody System
| Applicant | NanoHive Medical, LLC, Woburn MA, US |
| Decision | Substantially Equivalent, Jul 12, 2023 |
| Received | Apr 28, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231241
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.