510(k) K211805 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
IdentiTi Porous Ti Interbody System, Transcend PEEK Interbody System, IdentiTi NanoTec Interbody System, Transcend NanoTec Interbody System
| Applicant | Alphatec Spine, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Sep 22, 2021 |
| Received | Jun 11, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211805
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.