FDA 510(k), K143668, Navio

FDA 510(k), K143668, Navio

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510(K) Number: K143668
Device Name: Navio
Manufacturer: BLUE BELT TECHNOLOGIES, INC.
Device Classification Name: orthopedic stereotaxic instrument
Regulation Number: 882.4560
Classification Product Code: OLO
Date Received: 12/24/2014
Decision Date: 03/20/2015
Regulation Medical Specialty: Neurology

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