510(k) K163180 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Hubble II
| Applicant | Orbbo Surgical, LLC, Los Angeles CA, US |
| Decision | Substantially Equivalent, Dec 29, 2016 |
| Received | Nov 14, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163180
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.