The following data is part of a premarket notification filed by Neoortho Productos Orthopedicos S/a with the FDA for Mini And Micro Fragments Reconstruction System-neofix.
Device ID | K142419 |
510k Number | K142419 |
Device Name: | Mini And Micro Fragments Reconstruction System-NEOFIX |
Classification | Plate, Fixation, Bone |
Applicant | NEOORTHO PRODUCTOS ORTHOPEDICOS S/A RUA ANGELO DOMINGOS DURIGAN, 607, CASCATINHA Curitiba, BR 82025-100 |
Contact | Mariana De Oliveira Quinzani |
Correspondent | Kevin A Thomas PAXMED INTERNATIONAL, LLC 12264 EL CAMINO REAL SUITE 400 San Diego, CA 92130 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-08-28 |
Decision Date | 2014-12-16 |
Summary: | summary |