FDA 510(k) Applications Submitted by HENRY KLYCE

FDA 510(k) Number Submission Date Device Name Applicant
K103383 11/18/2010 SPARTEK VARIABLE ANGLE PEDICLE SCREW POSTERIOR FUSION SYSTEM SPARTEK MEDICAL, INC.
K094002 12/28/2009 SPARTEK VARIABLE ANGLE PEDICLE SCREW POSTERIOR FUSION SYSTEM SPARTEK MEDICAL, INC.


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