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FDA 510(k) Applications Submitted by MANAS M LELE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K161370
05/17/2016
Durepair Dura Regeneration Matrix
Medtronic Neurosurgery
K131101
04/19/2013
ITERO SOFTWARE
CADENT, LTD. AN ALIGN TECHNOLOGY COMPANY
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