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FDA 510(k), K120691, BRAIN PORT
FDA 510(k), K120691, BRAIN PORT
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510(K) Number: K120691
Device Name: BRAIN PORT
Manufacturer: NICO CORPORATION
Device Classification Name: retractor, self-retaining, for neurosurgery
Regulation Number: 882.4800
Classification Product Code: GZT
Date Received: 03/07/2012
Decision Date: 06/05/2012
Regulation Medical Specialty: Neurology
Device Name: BRAIN PORT
Manufacturer: NICO CORPORATION
Device Classification Name: retractor, self-retaining, for neurosurgery
Regulation Number: 882.4800
Classification Product Code: GZT
Date Received: 03/07/2012
Decision Date: 06/05/2012
Regulation Medical Specialty: Neurology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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