510(k) K111774 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PATHWAY MODEL 07XXXX
| Applicant | Custom Spine, Parsippany NJ, US |
| Decision | Substantially Equivalent, Jul 20, 2011 |
| Received | Jun 23, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K111774
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.