510(k) K232069 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Expandable Lumbar Fusion Cage (Type I,Type II)
| Applicant | Shanghai Reach Medical Instrument Co, Ltd., Shanghai, CN |
| Decision | Substantially Equivalent, Nov 29, 2023 |
| Received | Jul 12, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232069
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.