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FDA 510(k) Applications Submitted by Contego Medical Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K221204
04/26/2022
Excipio SV Thrombectomy Device
Contego Medical Inc.
K221339
05/09/2022
Paladin Carotid Post-Dilation Balloon System with Integrated Embolic Protection
Contego Medical Inc.
K223897
12/28/2022
Excipio LV Thrombectomy Device
Contego Medical Inc.
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