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.
Device ID | K141103 |
510k Number | K141103 |
Device Name: | INTRAMEDULLARY NAIL AND SCREWS-NEONAIL |
Classification | Rod, Fixation, Intramedullary And Accessories |
Applicant | NEOORTHO PRODUTOS ORTOPEDICOS S/A 11234 EL CAMINO REAL SUITE 400 San Diego, CA 92130 |
Contact | Kevin A Thomas |
Correspondent | Kevin A Thomas NEOORTHO PRODUTOS ORTOPEDICOS S/A 11234 EL CAMINO REAL SUITE 400 San Diego, CA 92130 |
Product Code | HSB |
CFR Regulation Number | 888.3020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-04-29 |
Decision Date | 2014-09-23 |
Summary: | summary |