Neoortho Productos Orthopedicos S/A
Country not established
- Devices
- 2
What Neoortho Productos Orthopedicos S/A makes
Neoortho Productos Ortopédicos S/A manufactures orthopedic fixation systems, including the Mini and Micro Fragments Reconstruction System-NEOFIX for bone fragment stabilization, and the NEOPLATE SPINE ANTERIOR FIXATION SYSTEM for spinal anterior stabilization.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Neoplate Spine Anterior Fixation System Ref K132653
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neoortho Productos Orthopedicos S/A have in the registry?
The registry currently lists 2 devices for Neoortho Productos Orthopedicos S/A. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neoortho Productos Orthopedicos S/A's devices?
Among its 2 most recently registered devices, Neoortho Productos Orthopedicos S/A has devices listed in FDA 510(k) (2 devices).
What risk classes do Neoortho Productos Orthopedicos S/A's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Neoortho Productos Orthopedicos S/A's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neoortho Productos Orthopedicos S/A in the registry?
The most recently registered devices listed for Neoortho Productos Orthopedicos S/A include Mini and Micro Fragments Reconstruction System-NEOFIX and NEOPLATE SPINE ANTERIOR FIXATION SYSTEM.