FDA 510(k), K200662, X-Guide® Surgical Navigation System

FDA 510(k), K200662, X-Guide® Surgical Navigation System

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510(K) Number: K200662
Device Name: X-Guide® Surgical Navigation System
Manufacturer: Fred Cowdery
Device Classification Name: Dental Stereotaxic Instrument
Regulation Number: PLV
Classification Product Code: 03/13/2020
Date Received: 05/21/2020
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental

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