The following data is part of a premarket notification filed by Neoortho Produtos Ortopedicos S/a with the FDA for Small And Large Fragments Osteosynthesis System Neofix.
Device ID | K113733 |
510k Number | K113733 |
Device Name: | SMALL AND LARGE FRAGMENTS OSTEOSYNTHESIS SYSTEM NEOFIX |
Classification | Plate, Fixation, Bone |
Applicant | NEOORTHO PRODUTOS ORTOPEDICOS S/A 11234 EL CAMINO REAL SUITE 200 San Diego, CA 92130 |
Contact | Kevin A Thomas |
Correspondent | Kevin A Thomas NEOORTHO PRODUTOS ORTOPEDICOS S/A 11234 EL CAMINO REAL SUITE 200 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 | 2011-12-19 |
Decision Date | 2012-03-23 |
Summary: | summary |