FDA 510(k) Application Details - K053424

Device Classification Name	Mesh, Surgical, Polymeric   More FDA Info for this Device
510(K) Number	K053424
Device Name	Mesh, Surgical, Polymeric
Applicant	CALDERA MEDICAL, INC. 28632 ROADSIDE DR., SUITE 260 AGOURA HILLS, CA 91301 US Other 510(k) Applications for this Company
Contact	MARLA KENGEN Other 510(k) Applications for this Contact
Regulation Number	878.3300   More FDA Info for this Regulation Number
Classification Product Code	FTL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/08/2005
Decision Date	02/22/2006
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