510(k) K163481 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
HALF DOME Posterior Lumbar Interbody System
| Applicant | Astura Medical, Carlsbad CA, US |
| Decision | Substantially Equivalent, May 3, 2017 |
| Received | Dec 12, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163481
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.