510(k) K171893 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Blustone Synergy Lumbar Interbody Fusion System (Basalt, Magma, Obsidian), Blustone Synergy Cervical Interbody Fusion System (Slate)
| Applicant | Bluestone Synergy, Pueblo CO, US |
| Decision | Substantially Equivalent, Sep 8, 2017 |
| Received | Jun 26, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171893
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.