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 |