510(k) K113540 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
RELIANCE LUMBAR IBF SYSTEM
| Applicant | Reliance Medical Systems, LLC, Bountiful UT, US |
| Decision | Substantially Equivalent, Mar 12, 2012 |
| Received | Nov 30, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113540
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.