510(k) K170512 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Altus Spine Titanium Interbody Fusion System
| Applicant | Altus Partners, LLC, West Chester PA, US |
| Decision | Substantially Equivalent, Mar 10, 2017 |
| Received | Feb 21, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K170512
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.