FDA 510(k) Applications Submitted by Roche Janse van Rensburg

FDA 510(k) Number Submission Date Device Name Applicant
K140853 04/03/2014 STIMPOD ST2-3010 NERVE STIMULATOR XAVANT TECHNOLOGY (PTY) LTD
K072092 07/30/2007 XPOD/XMAP NERVE STIMULATOR XAVANT TECHNOLOGY (PTY), LTD.
K213049 09/22/2021 STIMPOD NMS450 Nerve Stimulator Xavant Technology (Pty) Ltd


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