510(k) K181347 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Aries® Lumbar Interbodies
| Applicant | Osseus Fusion Systems, LLC, Dallas TX, US |
| Decision | Substantially Equivalent, Aug 15, 2018 |
| Received | May 21, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181347
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.