510(k) K251479 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Mobarn 80:20 Lumbar Interbody Fusion System (Posterior Lumbar Interbody Fusion Cage (PLIF)); Mobarn 80:20 Lumbar Interbody Fusion System (Transforaminal Lumbar Interbody Fusion Cage (TLIF)); Mobarn 80:20 Lumbar Interbody Fusion System (Direct Lateral Lumbar Interbody Fusion Cage (DLIF)); Mobarn 80:2
| Applicant | Mobarn Medical Devices, LLC, New Orleans LA, US |
| Decision | Substantially Equivalent, Sep 18, 2025 |
| Received | May 13, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251479
No recall in the FDA data names this 510(k).
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