FDA 510(k) Applications for Medical Device Product Code: KAM (Cannula, Sinus)

FDA 510(k) Applications for Medical Device Product Code "KAM"
(Cannula, Sinus)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K062458	ACCLARENT, INC.	ETHMOID SINUS SPACER	09/15/2006
K093594	ACCLARENT, INC.	MODIFICATION TO RELIEVA STRATUS MICROFLOW SPACER	03/03/2010
K060974	ACCLARENT, INC.	RELIENT NAVIGATION DEVICE	05/05/2006
K073041	ACCLARENT, INC.	RELIEVA AND RELIEVA ACELLA SINUS BALLOON CATHETER	03/11/2008
K071845	ACCLARENT, INC.	RELIEVA LUMA SINUS ILLUMINATION SYSTEM, MODEL SIS-100A	09/28/2007
K083574	ACCLARENT, INC.	RELIEVA STRATUS MICROFLOW SPACER	01/29/2009
K110687	ACCLARENT, INC.	RELIEVA STRATUS PRO MICROFLOW SPACER (FRONTAL)	10/07/2011
K072891	ACCLARENT, INC.	SINUS SPACER	03/19/2008
K050340	MICROMEDICS, INC.	MICROMEDICS SPHENOID SINUS STENT	04/27/2005
K994262	XOMED, INC.	FRONTAL SINUS TREPHINATION CANNULA	02/08/2000
K973273	XOMED, INC.	XOMED T-STENT, FRONTAL SINUS STENT	09/29/1997