510(k) K182608 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Oyster ACIF Cage
| Applicant | Silony Medical GmbH, Leinfelden-Echterdingen, DE |
| Decision | Substantially Equivalent, Jun 13, 2019 |
| Received | Sep 21, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182608
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.