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enVVeno Medical Presents Positive Preliminary Device Related Material Adverse Event (MAE) Data from the VenoValve Pivotal Trial at the 50th Annual VEITH Symposium

enVVeno Medical Presents Positive Preliminary Device Related Material Adverse Event (MAE) Data from the VenoValve Pivotal Trial at the 50th Annual VEITH Symposium
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New yorkUnited statesJenene thomasRobert bermanVveno medical corporation the companyDrug administrationVveno medical corporationClinical events committeeExchange commissionVveno medical corporation nasdaqPulmonary embolisms occurring duringFully enrolledMedical corporationMaterial adverse eventChronic venous insufficiencyData safety monitoring board

enVVeno Medical Presents Positive Preliminary Device Related Material Adverse Event (MAE) Data from the VenoValve Pivotal Trial at the 50th Annual VEITH Symposium

enVVeno Medical Presents Positive Preliminary Device Related Material Adverse Event (MAE) Data from the VenoValve Pivotal Trial at the 50th Annual VEITH Symposium
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United statesNew yorkRobert bermanJenene thomasVveno medical corporation the companyVveno medical corporationDrug administrationExchange commissionClinical events committeeVveno medical corporation nasdaqPulmonary embolisms occurring duringFully enrolledMedical corporationMaterial adverse eventChronic venous insufficiencyData safety monitoring board

enVVeno Medical Presents Positive Preliminary Device Related Material Adverse Event (MAE) Data from the VenoValve Pivotal Trial at the 50th Annual VEITH Symposium

enVVeno Medical Presents Positive Preliminary Device Related Material Adverse Event (MAE) Data from the VenoValve Pivotal Trial at the 50th Annual VEITH Symposium
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United statesNew yorkRobert bermanJenene thomasClinical events committeeDrug administrationVveno medical corporation nasdaqVveno medical corporation the companyVveno medical corporationExchange commissionPulmonary embolisms occurring duringFully enrolledMedical corporationMaterial adverse eventChronic venous insufficiencyData safety monitoring board

InspireMD Presents Positive 30-Day Follow-Up Results from the C-GUARDIANS U S Investigational Device Exemption (IDE) Clinical Trial at VIVA23

InspireMD Presents Positive 30-Day Follow-Up Results from the C-GUARDIANS U S Investigational Device Exemption (IDE) Clinical Trial at VIVA23
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United statesMarvin slosmanChuck padalaChris metzgerLas vegasInspiremd incClinical events committeeExchange commissionCompany annual report on formDay follow up resultsDevice exemptionClinical trialEmbolic prevention stent systemVascular interventional advancesSystem vascular chiefCarotid stent system

InspireMD Presents Positive 30-Day Follow-Up Results from the C-GUARDIANS U S Investigational Device Exemption (IDE) Clinical Trial at VIVA23

TEL AVIV, Israel and MIAMI, Nov. 01, 2023 InspireMD, Inc. , developer of the CGuard™ Embolic Prevention Stent System for the prevention of stroke, today presented 30-day results from the.

United statesLas vegasChris metzgerMarvin slosmanChuck padalaGlobenewswire incInspiremd incExchange commissionCompany annual report on formClinical events committeeEmbolic prevention stent systemDevice exemptionVascular interventional advancesSystem vascular chiefCarotid stent systemPremarket approval