510(k) K150285 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Leva(TM) Spacer System
| Applicant | Spine Wave, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Mar 5, 2015 |
| Received | Feb 5, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K150285
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.