510(k) K183447 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
EIT Cellular Titanium Lumbar Cage - T/PLIF
| Applicant | Eit Emerging Implant Technologies GmbH, Wurmlingen, DE |
| Decision | Substantially Equivalent, Feb 4, 2019 |
| Received | Dec 12, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183447
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.