510(k) K213417 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Ghost Spacer System
| Applicant | Life Spine, Inc., Huntley IL, US |
| Decision | Substantially Equivalent, Sep 29, 2022 |
| Received | Oct 20, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213417
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.