510(k) K181548 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Pantheon Spinal Pontus Interbody Fusion Device
| Applicant | Pantheon Spinal, Austin TX, US |
| Decision | Substantially Equivalent, Dec 16, 2019 |
| Received | Jun 12, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181548
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.