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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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