고객지원공지사항
작성자 admin 날짜 2020-09-09
이메일 bkm@bkmeditech.com
제목 FDA Approval of Mega Plus MIS Spine System
- 510(k) Number: K200981
- Trade/ Device Name: Mega Plus MIS Spine System
- Regulation Number: 21 CFR 888.3070
- Regulation Name: Thoracolumbosacral Pedicle Screw System
- Regulatory Class: Class II
- Product Code: NKB
- Dated: July 10, 2020