510(k) K212540 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Explorer TO System
| Applicant | SeaSpine Orthopedics Corporation, Carlsbad CA, US |
| Decision | Substantially Equivalent, Sep 10, 2021 |
| Received | Aug 12, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K212540
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.