FDA 510(k), K171651, EXCELSIUS GPS

510(K) Number: K171651
Device Name: EXCELSIUS GPS
Manufacturer: Globus Medical Inc.
Device Classification Name: Orthopedic Stereotaxic Instrument
Regulation Number: 882.4560
Classification Product Code: OLO
Date Received: 06/05/2017
Decision Date: 08/16/2017
Regulation Medical Specialty: Neurology

223 pages (2,090 of 2,207 original pages are fully redacted)