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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact