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 |