510(k) K142269 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Reliance Cervical IBF System
| Applicant | Reliance Medical Systems, LLC, Bountiful UT, US |
| Decision | Substantially Equivalent, Jun 9, 2015 |
| Received | Aug 15, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142269
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.