510(k) K231275 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Exceed Biplanar Expandable Interbody System
| Applicant | Spine Wave, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Jul 25, 2023 |
| Received | May 2, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231275
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.