510(k) K180687 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Reliance Lumber IBF System
| Applicant | Reliance Medical Systems, Bountiful UT, US |
| Decision | Substantially Equivalent, May 15, 2018 |
| Received | Mar 15, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K180687
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.