FDA 510(k) Application Details - K072870

Device Classification Name	System, Ablation, Microwave And Accessories   More FDA Info for this Device
510(K) Number	K072870
Device Name	System, Ablation, Microwave And Accessories
Applicant	FOUNDRY NEWCO X, INC. 199 JEFFERSON DRIVE MENLO PARK, CA 94025 US Other 510(k) Applications for this Company
Contact	GREGORY MATHISON Other 510(k) Applications for this Contact
Regulation Number	878.4400   More FDA Info for this Regulation Number
Classification Product Code	NEY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/09/2007
Decision Date	01/14/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review