510(k) K103743 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
CONCORDE CURVE SYSTEM
| Applicant | Johnson & Johnson, Raynham MA, US |
| Decision | Substantially Equivalent, Mar 17, 2011 |
| Received | Dec 23, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K103743
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.