Bk Meditech, Co., Ltd. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Bk Meditech, Co., Ltd. has 11 FDA 510(k) cleared orthopedic devices. Based in Hwasung-Si, Kyunggi-Do, KR.
Historical record: 11 cleared submissions from 2006 to 2020.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Bk Meditech, Co., Ltd.
11 devices
Cleared
Aug 11, 2020
Mega Plus MIS Spine System
Orthopedic
119d
Cleared
Dec 10, 2018
Mega Plus Spine System
Orthopedic
35d
Cleared
Mar 15, 2018
Mega Plus Spine System
Orthopedic
167d
Cleared
Oct 01, 2014
INNESIS PEEK TL CAGE
Orthopedic
209d
Cleared
Apr 02, 2014
INNESIS PEEK CERVICAL CAGE
Orthopedic
237d
Cleared
Jan 18, 2013
INNESIS PEEK CAGE
Orthopedic
338d
Cleared
Nov 02, 2011
DYNA-EXTOR II
Orthopedic
261d
Cleared
May 14, 2009
DVX SPINE SYSTEM
Orthopedic
84d
Cleared
Jun 04, 2008
DVX SPINE SYSTEM
Orthopedic
65d
Cleared
Nov 01, 2007
MEGA SPINE SYSTEM
Orthopedic
63d
Cleared
Jul 26, 2006
PIN SCREW
Orthopedic
48d