510(k) K134038 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
CAMBER SPINE DIAGON OBLIQUE CAGE
| Applicant | Camber Spine, Newtown Square PA, US |
| Decision | Substantially Equivalent, Mar 20, 2014 |
| Received | Dec 31, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K134038
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.