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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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