510(k) K193255 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Largo PEEK Interbody System
| Applicant | Flospine, LLC, Boca Raton FL, US |
| Decision | Substantially Equivalent, Feb 20, 2020 |
| Received | Nov 26, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193255
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.