FDA 510(k) Application Details - K022907

Device Classification Name	Rongeur, Powered   More FDA Info for this Device
510(K) Number	K022907
Device Name	Rongeur, Powered
Applicant	THE ANSPACH EFFORT, INC. 4500 RIVERSIDE DR. PALM BEACH GARDENS, FL 33410 US Other 510(k) Applications for this Company
Contact	WILLIAM G CONETY Other 510(k) Applications for this Contact
Regulation Number	882.4845   More FDA Info for this Regulation Number
Classification Product Code	HAD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/03/2002
Decision Date	10/21/2002
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