510(k) K172947 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
HALF DOME Posterior Lumbar Interbody System
| Applicant | Astura Medical, Carlsbad CA, US |
| Decision | Substantially Equivalent, Apr 18, 2018 |
| Received | Sep 26, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K172947
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.