FDA 510(k) Applications Submitted by RENISHAW MAYFIELD SARL

FDA 510(k) Number Submission Date Device Name Applicant
K180206 01/24/2018 neuromate Gen III Renishaw Mayfield Sarl
K181706 06/28/2018 neuromate Gen III Renishaw Mayfield Sarl
K132755 09/03/2013 NEUROMATE FRAMELESS GEN II RENISHAW MAYFIELD SARL


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