The following data is part of a premarket notification filed by Fixier, S.a. De C.v. with the FDA for Traufix Osteosynthesis, Osteotomy, And Arthrodesis Devices.
Device ID | K201510 |
510k Number | K201510 |
Device Name: | Traufix Osteosynthesis, Osteotomy, And Arthrodesis Devices |
Classification | Plate, Fixation, Bone |
Applicant | Fixier, S.A. De C.V. Calle Joaquín Pardavé No. 223 Colonia Casa Blanca Leon, MX C.p. 37170 |
Contact | Vianey Mariana Perez Suarez |
Correspondent | Aurelia Brownridge Aurelia Brownridge 11594 Cesped Drive San Diego, CA 92124 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2020-06-05 |
Decision Date | 2022-02-18 |