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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