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 |