510(k) K233375 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Tranquil-L Interbody System
| Applicant | Nexus Spine, LLC, Salt Lake City UT, US |
| Decision | Substantially Equivalent, Mar 20, 2024 |
| Received | Oct 2, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K233375
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.