510(k) K232619 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
MATRIX HA PEEK Cervical IBF System
| Applicant | Sapphire Medical Group, Dana Point CA, US |
| Decision | Substantially Equivalent, Mar 19, 2024 |
| Received | Aug 29, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K232619
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.