510(k) K173606 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
SeaSpine Vu aPOD Prime NanoMetalene Intervertebral Body Fusion Device, SeaSpine Vu aPOD Prime Intervertebral Body Fusion Device
| Applicant | SeaSpine Orthopedics Corporation, Carlsbad CA, US |
| Decision | Substantially Equivalent, Apr 13, 2018 |
| Received | Nov 21, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173606
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.