510(k) K181531 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices
| Applicant | Spineex, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Oct 5, 2018 |
| Received | Jun 11, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181531
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.