Mobarn Medical Devices, LLC - FDA 510(k) Cleared Devices
Recent clearances: Mobarn 80:20 Lumbar Interbody Fusion System (Posterior Lumbar Interbody Fusion Cage (PLIF))
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Mobarn Medical Devices, LLC Orthopedic ✕
1 devices