510(k) K233694 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Meridian Interbody System; WaveForm A Interbody System
| Applicant | SeaSpine Orthopedics Corporation, Carlsbad CA, US |
| Decision | Substantially Equivalent, Jan 12, 2024 |
| Received | Nov 17, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233694
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.