510(k) K220711 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SeaSpine Meridian System, SeaSpine Meridian Anterior Plate System
| Applicant | SeaSpine Orthopedics Corporation, Carlsbad CA, US |
| Decision | Substantially Equivalent, May 10, 2022 |
| Received | Mar 11, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220711
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.