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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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