510(k) K151756 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
STERISPINE LC CAGE
| Applicant | Safe Orthopaedics, Eragny Sur Oise, FR |
| Decision | Substantially Equivalent, Aug 21, 2015 |
| Received | Jun 29, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151756
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.