INTRAMEDULLARY NAIL AND SCREWS-NEONAIL

Rod, Fixation, Intramedullary And Accessories

NEOORTHO PRODUTOS ORTOPEDICOS S/A

The following data is part of a premarket notification filed by Neoortho Produtos Ortopedicos S/a with the FDA for Intramedullary Nail And Screws-neonail.

Pre-market Notification Details

Device IDK141103
510k NumberK141103
Device Name:INTRAMEDULLARY NAIL AND SCREWS-NEONAIL
ClassificationRod, Fixation, Intramedullary And Accessories
Applicant NEOORTHO PRODUTOS ORTOPEDICOS S/A 11234 EL CAMINO REAL SUITE 400 San Diego,  CA  92130
ContactKevin A Thomas
CorrespondentKevin A Thomas
NEOORTHO PRODUTOS ORTOPEDICOS S/A 11234 EL CAMINO REAL SUITE 400 San Diego,  CA  92130
Product CodeHSB  
CFR Regulation Number888.3020 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2014-04-29
Decision Date2014-09-23
Summary:summary

NIH GUDID Devices

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