Neoortho Produtos Ortopedicos S/A is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neoortho Produtos Ortopedicos S/A - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Neoortho Produtos Ortopedicos S/A has 5 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 5 cleared submissions from 2010 to 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Neoortho Produtos Ortopedicos S/A Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neoortho Produtos Ortopedicos S/A
5 devices
Cleared
Jun 27, 2017
Cannulated Screws Neoortho
Orthopedic
257d
Cleared
Sep 23, 2014
INTRAMEDULLARY NAIL AND SCREWS-NEONAIL
Orthopedic
147d
Cleared
May 29, 2014
PEEK CAGE FOR THE VERTEBRAL SPINE
Orthopedic
260d
Cleared
Mar 23, 2012
SMALL AND LARGE FRAGMENTS OSTEOSYNTHESIS SYSTEM NEOFIX
Orthopedic
95d
Cleared
Dec 20, 2010
MINI AND MICRO FRAGMENTS RECONSTRUCTION SYSTEM-NEOFACE
Dental
98d