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FDA 510(k), K093919, MICROPLEX COIL SYSTEM-COSMOS MODEL 100933CSSR-V, 101036CSSR-V, 101141CSSR-V, 101245CSSR-V
FDA 510(k), K093919, MICROPLEX COIL SYSTEM-COSMOS MODEL 100933CSSR-V, 101036CSSR-V, 101141CSSR-V, 101245CSSR-V
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510(K) Number: K093919
Device Name: MICROPLEX COIL SYSTEM-COSMOS MODEL 100933CSSR-V, 101036CSSR-V, 101141CSSR-V, 101245CSSR-V
Manufacturer: MICROVENTION, INC.
Device Classification Name: device, neurovascular embolization
Regulation Number: 882.5950
Classification Product Code: HCG
Date Received: 12/22/2009
Decision Date: 01/21/2010
Regulation Medical Specialty: Neurology
Device Name: MICROPLEX COIL SYSTEM-COSMOS MODEL 100933CSSR-V, 101036CSSR-V, 101141CSSR-V, 101245CSSR-V
Manufacturer: MICROVENTION, INC.
Device Classification Name: device, neurovascular embolization
Regulation Number: 882.5950
Classification Product Code: HCG
Date Received: 12/22/2009
Decision Date: 01/21/2010
Regulation Medical Specialty: Neurology
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- Delivery: Approximately 1 to 2 weeks
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