510(k) K241605 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Adaptix PEEK Interbody System with Nanotechnology; Capstone Control PEEK Spinal System with Nanotechnology
| Applicant | Nanovis, LLC, Columbia City IN, US |
| Decision | Substantially Equivalent, Sep 5, 2024 |
| Received | Jun 4, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241605
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.