510(k) K190193 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SpineEX Sagittae® Lateral Lumbar Interbody Fusion Devices
| Applicant | Spineex, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Mar 4, 2019 |
| Received | Feb 4, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K190193
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.