510(k) K161710 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SAGICO IBF SYSTEM ARIA LUMBAR, SAGICO IBF SYSTEM ARION CERVICAL
| Applicant | Spinal Analytics & Geometrical Impant Co, LLC, Tampa FL, US |
| Decision | Substantially Equivalent, Jun 29, 2017 |
| Received | Jun 21, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161710
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.