510(k) K210583 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SeaSpine WaveForm A Interbody System
| Applicant | SeaSpine Orthopedics Corporation, Carlsbad CA, US |
| Decision | Substantially Equivalent, Jun 2, 2021 |
| Received | Feb 26, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210583
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.