FDA 510(k) Applications Submitted by ATLAS SPINE INC.

FDA 510(k) Number Submission Date Device Name Applicant
K100743 03/16/2010 ATLAS SPINE PIVOTING SYSTEM ATLAS SPINE INC.
K110842 03/25/2011 ATLAS SPINE PEDICLE SCREW SYSTEM ATLAS SPINE INC.
K071497 05/31/2007 ATLAS SPINE VERTEBRAL BODY REPLACEMENT ATLAS SPINE INC.
K081880 07/02/2008 ATLAS SPINE SPACER ATLAS SPINE INC.
K063464 11/16/2006 ATLAS SPINE VERTEBRAL BODY REPLACEMENT ATLAS SPINE INC.
K112759 09/22/2011 APCLO PEDICLE SCREW SYSTEMS ATLAS SPINE INC.


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