510(k) K211873 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PSX Interbody System
| Applicant | Alphatec Spine, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Aug 10, 2021 |
| Received | Jun 17, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211873
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.