510(k) K192316 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Matrix HA PEEK Cervical Implant System
| Applicant | Sapphire Medical Group, Dana Point CA, US |
| Decision | Substantially Equivalent, Oct 17, 2019 |
| Received | Aug 26, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K192316
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.