The following data is part of a premarket notification filed by Syntec Scientific Corporation with the FDA for Syntec Femoral Nail System.
Device ID | K181296 |
510k Number | K181296 |
Device Name: | Syntec Femoral Nail System |
Classification | Rod, Fixation, Intramedullary And Accessories |
Applicant | Syntec Scientific Corporation No.2, Kung San Road, Chuan Shing Industrial Zone, Shen Kang Chang Hua, TW 50971 |
Contact | Nicole Tseng |
Correspondent | Nicole Tseng Syntec Scientific Corporation - Taipei Office 3F., No.96, Sec.3, Zhongxio East Road Da'An Dist. Taipei, TW 10652 |
Product Code | HSB |
CFR Regulation Number | 888.3020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-05-16 |
Decision Date | 2019-04-11 |