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 |