FDA 510(k), K111520, IPC POWEREASE SYSTEM
FDA 510(k), K111520, IPC POWEREASE SYSTEM
Device Name: IPC POWEREASE SYSTEM
Manufacturer: MEDTRONIC XOMED, INC.
Device Classification Name: Drills, Burrs, Trephines & Accessories (Simple, Powered)
Regulation Number: 882.4310
Classification Product Code: HBE
Date Received: 06/02/2011
Decision Date: 10/26/2011
Regulation Medical Specialty: Neurology
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