510(k) K181118 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Reliance Lumbar IBF System
| Applicant | Reliance Medical Systems, Bountiful UT, US |
| Decision | Substantially Equivalent, Jan 9, 2019 |
| Received | Apr 27, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181118
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.