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 |