510(k) K183705 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
IdentiTi Porous Ti Interbody System
| Applicant | Alphatec Spine, Inc., Carlsnad CA, US |
| Decision | Substantially Equivalent, Mar 1, 2019 |
| Received | Dec 31, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183705
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.