FDA 510(k) Applications Submitted by LEADER ITALIA S.R.L.

FDA 510(k) Number Submission Date Device Name Applicant
K062931 09/28/2006 IMPLUS IMPLANT SYSTEM LEADER ITALIA S.R.L.
K120792 03/15/2012 TIXOS IMPLANT SYSTEM LEADER ITALIA S.R.L.


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