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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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