FDA 510(k) Application Details - K090112

Device Classification Name	Motor, Drill, Pneumatic   More FDA Info for this Device
510(K) Number	K090112
Device Name	Motor, Drill, Pneumatic
Applicant	MEDTRONIC POWERED SURGICAL SOLUTIONS 4620 NORTH BEACH ST. FORT WORTH, TX 76137 US Other 510(k) Applications for this Company
Contact	JEFFERY HENDERSON Other 510(k) Applications for this Contact
Regulation Number	882.4370   More FDA Info for this Regulation Number
Classification Product Code	HBB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/16/2009
Decision Date	03/26/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review