510(k) K172888 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
EIT Cellular Titanium® Cervical Cages, EIT Cellular Titanium® PLIF Cages, EIT Cellular Titanium® TLIF Cages, EIT Cellular Titanium® ALIF Cages
| Applicant | Eit Emerging Implant Technologies GmbH, Wurmlingen, DE |
| Decision | Substantially Equivalent, Dec 15, 2017 |
| Received | Sep 21, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172888
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.