FDA 510(k) Applications Submitted by Synthes (USA) LLC

FDA 510(k) Number Submission Date Device Name Applicant
K180821 03/30/2018 TruMatch Graft Cage - Long Bone Synthes (USA) LLC
K120275 01/30/2012 SYNTHES ACIS/VERTEBRAL SPACER CR SYNTHES (USA) LLC
K101536 06/03/2010 2.7/3.5MM VA-LCP ANTERIRO CLAVICLE PLATE SYSTEM SYNTHES (USA) LLC
K130146 01/22/2013 SYNTHES SYNFLATE VERTEVRAL BALLOON SYSTEM SYNTHES (USA) LLC


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