510(k) K181899 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ROCCIA® PLIF
| Applicant | Silony Medical GmbH, Leinfelden-Echterdingen, DE |
| Decision | Substantially Equivalent, Dec 13, 2018 |
| Received | Jul 16, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181899
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.