510(k) K173283 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Reliance Lumbar IBF System
| Applicant | Reliance Medical Systems, LLC, Bountiful UT, US |
| Decision | Substantially Equivalent, Jan 19, 2018 |
| Received | Oct 16, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K173283
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.