FDA 510(k), K182531, ClotTriever Thrombectomy System
FDA 510(k), K182531, ClotTriever Thrombectomy System
510(K) Number: K182531
Device Name: ClotTriever Thrombectomy System
Manufacturer: Inari Medical
Device Classification Name: Peripheral Mechanical Thrombectomy With Aspiration
Regulation Number: 870.5150
Classification Product Code: QEW
Date Received: 09/14/2018
Decision Date: 10/10/2018
Regulation Medical Specialty: Cardiovascular
Total pages: 108
Fully redacted pages: 88
Content pages: 20
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