FDA 510(k) Application Details - K071745

Device Classification Name	Probe, Radiofrequency Lesion   More FDA Info for this Device
510(K) Number	K071745
Device Name	Probe, Radiofrequency Lesion
Applicant	BAYLIS MEDICAL CO., INC. 2645 MATHESON BLVD. E MISSISSAUGA, ONTARIO L4W 5S4 CA Other 510(k) Applications for this Company
Contact	MEGHAL KHAKHAR Other 510(k) Applications for this Contact
Regulation Number	882.4725   More FDA Info for this Regulation Number
Classification Product Code	GXI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/27/2007
Decision Date	07/19/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review