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FDA 510(k) Applications Submitted by BK MEDITECH Co., Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K173180
09/29/2017
Mega Plus Spine System
BK MEDITECH Co., Ltd.
K061599
06/08/2006
PIN SCREW
BK MEDITECH CO., LTD.
K110426
02/14/2011
DYNA-EXTOR II
BK MEDITECH CO., LTD.
K090424
02/19/2009
DVX SPINE SYSTEM
BK MEDITECH CO., LTD.
K140577
03/06/2014
INNESIS PEEK TL CAGE
BK MEDITECH CO., LTD.
K080876
03/31/2008
DVX SPINE SYSTEM
BK MEDITECH CO., LTD.
K132483
08/08/2013
INNESIS PEEK CERVICAL CAGE
BK MEDITECH CO., LTD.
K072436
08/30/2007
MEGA SPINE SYSTEM
BK MEDITECH CO., LTD.
K120464
02/15/2012
INNESIS PEEK CAGE
BK MEDITECH CO., LTD.
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