Medical Device Manufacturer · US , Aventura , FL

Neoortho Productos Orthopedicos S/A - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2014
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.

FDA 510(k) Regulatory Record - Neoortho Productos Orthopedicos S/A
2 devices
1-2 of 2
Cleared Dec 16, 2014
Mini and Micro Fragments Reconstruction System-NEOFIX
K142419 · HRS
Orthopedic · 110d
Cleared May 14, 2014
NEOPLATE SPINE ANTERIOR FIXATION SYSTEM
K132653 · KWQ
Orthopedic · 261d
Filters
Filter by Specialty
All2 Orthopedic 2