Neoortho Productos Orthopedicos S/A is one of 18477 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neoortho Productos Orthopedicos S/A - FDA 510(k) Cleared Devices
Recent clearances: Mini and Micro Fragments Reconstruction System-NEOFIX, NEOPLATE SPINE ANTERIOR FIXATION SYSTEM
2
Total
2
Cleared
0
Denied
Neoortho Productos Orthopedicos S/A has 2 FDA 510(k) cleared medical devices. Based in Aventura, US.
Historical record: 2 cleared submissions from 2014 to 2014. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Neoortho Productos Orthopedicos S/A Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by PaxMed International, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Neoortho Productos Orthopedicos S/A
2 devices