510(k) K203003 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Pantheon IBFD
| Applicant | Pantheon Spinal, Georgetown TX, US |
| Decision | Substantially Equivalent, Jul 7, 2021 |
| Received | Oct 1, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K203003
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.