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Retropsoas Technologies, LLC

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K242457 EARP Interbody SystemMAX2024-10-07 View
510(k) K241917 EARP Nerve Cuff ElectrodeETN2024-07-31 View
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