510(k) K173102 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Reliance Cervical IBF System
| Applicant | Reliance Medical Systems, LLC, Bountiful UT, US |
| Decision | Substantially Equivalent, Dec 29, 2017 |
| Received | Sep 29, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K173102
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.