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FDA 510(k), K110010, NEUROPORT CORTICAL MICROELECTRODE ARRAY SYSTEM
FDA 510(k), K110010, NEUROPORT CORTICAL MICROELECTRODE ARRAY SYSTEM
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510(K) Number: K110010
Device Name: NEUROPORT CORTICAL MICROELECTRODE ARRAY SYSTEM
Manufacturer: BLACKROCK MICROSYSTEMS, INC
Device Classification Name: electrode, depth
Regulation Number: 882.1330
Classification Product Code: GZL
Date Received: 01/03/2011
Decision Date: 02/09/2011
Regulation Medical Specialty: Neurology
Device Name: NEUROPORT CORTICAL MICROELECTRODE ARRAY SYSTEM
Manufacturer: BLACKROCK MICROSYSTEMS, INC
Device Classification Name: electrode, depth
Regulation Number: 882.1330
Classification Product Code: GZL
Date Received: 01/03/2011
Decision Date: 02/09/2011
Regulation Medical Specialty: Neurology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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