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FDA 510(k), K151359, ROSA Brain
FDA 510(k), K151359, ROSA Brain
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510(K) Number: K151359
Device Name: ROSA Brain
Manufacturer: MICHAEL CHRIST
Device Classification Name: Neurological Stereotaxic Instrument
Regulation Number: HAW
Classification Product Code: 05/20/2015
Date Received: 12/18/2015
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
Device Name: ROSA Brain
Manufacturer: MICHAEL CHRIST
Device Classification Name: Neurological Stereotaxic Instrument
Regulation Number: HAW
Classification Product Code: 05/20/2015
Date Received: 12/18/2015
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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