510(k) K170553 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Altus Spine Interbody Fusion System
| Applicant | Altus Partners, LLC, West Chester PA, US |
| Decision | Substantially Equivalent, Dec 1, 2017 |
| Received | Feb 24, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170553
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.