510(k) K232996 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF)
| Applicant | Shanghai Iatrical-Ti Technologies CO , Ltd., Shanghai, CN |
| Decision | Substantially Equivalent, Sep 6, 2024 |
| Received | Sep 22, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232996
No recall in the FDA data names this 510(k).
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