The following data is part of a premarket notification filed by Neoortho Produtos Ortopedicos S/a with the FDA for Mini And Micro Fragments Reconstruction System-neoface.
| Device ID | K102641 |
| 510k Number | K102641 |
| Device Name: | MINI AND MICRO FRAGMENTS RECONSTRUCTION SYSTEM-NEOFACE |
| Classification | Plate, Bone |
| Applicant | NEOORTHO PRODUTOS ORTOPEDICOS S/A 11234 EL CAMINO REAL SUITE 200 San Diego, CA 92130 |
| Contact | Linda K Schulz |
| Correspondent | Linda K Schulz NEOORTHO PRODUTOS ORTOPEDICOS S/A 11234 EL CAMINO REAL SUITE 200 San Diego, CA 92130 |
| Product Code | JEY |
| CFR Regulation Number | 872.4760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-09-13 |
| Decision Date | 2010-12-20 |
| Summary: | summary |