FDA 510(k) Application Details - K003612

Device Classification Name	Motor, Drill, Electric   More FDA Info for this Device
510(K) Number	K003612
Device Name	Motor, Drill, Electric
Applicant	AESCULAP, INC. 3773 EXECUTIVE CENTER PKWY. CENTER VALLEY, PA 18034 US Other 510(k) Applications for this Company
Contact	JOYCE THOMAS Other 510(k) Applications for this Contact
Regulation Number	882.4360   More FDA Info for this Regulation Number
Classification Product Code	HBC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/22/2000
Decision Date	02/20/2001
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