FDA 510(k) K153203, Navigation Instruments, by Globus Medical, Inc.

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510(K) Number: K153203 Device Name: Navigation Instruments Manufacturer: Globus Medical, Inc.Device Classification Name: Orthopedic Stereotaxic Instrument Regulation Number: 882.45 60 Classification Product Code: OLO Date Received: 11/04/2015 Decision Date: 02/03/2016 Regulation Medical Specialty: Neurology Show more