510(k) K162351 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
SeaSpine® Vu aPOD Prime NanoMetalene® Intervertebral Body Fusion Device
| Applicant | SeaSpine Orthopedics Corporation, Carlsbad CA, US |
| Decision | Substantially Equivalent, Dec 1, 2016 |
| Received | Aug 23, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162351
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.