510(k) K101923 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
CONCORDE CURVE SYSTEM
| Applicant | Depuy Spine, Raynham MA, US |
| Decision | Substantially Equivalent, Dec 1, 2010 |
| Received | Jul 9, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101923
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.