510(k) K121254 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
CAMBER SPINE TECHNOLOGIES TLS 5.0 INERBODY CAGE
| Applicant | Camber Spine Technologies, Newtown Square PA, US |
| Decision | Substantially Equivalent, Jan 11, 2013 |
| Received | Apr 25, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121254
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.