The following data is part of a premarket notification filed by Baui Biotech Co., Ltd. with the FDA for Nova Minimally Invasive System.
Device ID | K182416 |
510k Number | K182416 |
Device Name: | NOVA Minimally Invasive System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | BAUI Biotech CO., LTD. 6F., No.8, Sec. 1, Zhongxing Rd., Wugu Dist. New Taipei City, TW 24872 |
Contact | Herman Jhan |
Correspondent | Herman Jhan BAUI Biotech CO., LTD. 6F., No.8, Sec. 1, Zhongxing Rd., Wugu Dist. New Taipei City, TW 24872 |
Product Code | NKB |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-09-04 |
Decision Date | 2019-06-11 |