510(k) K171434 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ROCCIA® MultiLIF
| Applicant | Silony Medical GmbH, Leinfelden-Echterdingen, DE |
| Decision | Substantially Equivalent, Dec 21, 2017 |
| Received | May 15, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171434
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.