510(k) K220296 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Manta Ray TDF Spacer
| Applicant | SeaSpine Orthopedics Corporation, Carlsbad CA, US |
| Decision | Substantially Equivalent, Feb 3, 2023 |
| Received | Feb 2, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220296
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.