510(k) K133893 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
STERISPINE LC CAGE
| Applicant | Safe Orthopaedics, Eragny Sur Oise, FR |
| Decision | Substantially Equivalent, Mar 14, 2014 |
| Received | Dec 20, 2013 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K133893
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.