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FDA 510(k) Applications Submitted by ORTHO-PRO LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K042310
08/25/2004
ORTHO-PRO CANNULATED BONE SCREWS
ORTHO-PRO LLC
K032682
08/29/2003
STS SCREW
ORTHO-PRO LLC
K102601
09/09/2010
ORTHOFLEX ROD
ORTHO-PRO LLC
K094037
12/30/2009
TC PLATING SYSTEM
ORTHO-PRO LLC
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