510(k) K152512 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Half Dome Posterior Lumbar Interbody System
| Applicant | Astura Medical, Carlsbad CA, US |
| Decision | Substantially Equivalent, Jan 28, 2016 |
| Received | Sep 2, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152512
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.