510(k) K131178 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
IDYS LIF CAGES
| Applicant | Clariance, Philedelphia PA, US |
| Decision | Substantially Equivalent, Oct 10, 2013 |
| Received | Apr 25, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131178
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.