FDA 510(k) Application Details - K020069

Device Classification Name	Motor, Drill, Pneumatic   More FDA Info for this Device
510(K) Number	K020069
Device Name	Motor, Drill, Pneumatic
Applicant	MEDTRONIC MIDAS REX 4620 NORTH BEACH ST. FORT WORTH, TX 76137 US Other 510(k) Applications for this Company
Contact	GREG CANNEDY 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	01/09/2002
Decision Date	03/18/2002
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