FDA 510(k), K153203, Navigation Instruments
FDA 510(k), K153203, Navigation Instruments
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510(K) Number: K153203
Device Name: Navigation Instruments
Manufacturer:
Device Classification Name: Orthopedic Stereotaxic Instrument
Regulation Number: 882.4560
Classification Product Code: OLO
Date Received: 11/04/2015
Decision Date: 02/03/2016
Regulation Medical Specialty: Neurology
Device Name: Navigation Instruments
Manufacturer:
Device Classification Name: Orthopedic Stereotaxic Instrument
Regulation Number: 882.4560
Classification Product Code: OLO
Date Received: 11/04/2015
Decision Date: 02/03/2016
Regulation Medical Specialty: Neurology