FDA 510(k) Applications Submitted by SYNOVIS SURGICAL INNOVATIONS

FDA 510(k) Number	Submission Date	Device Name	Applicant
K040119	01/20/2004	PERI-STRIPS STAPLE LINE REINFORCEMENT-SLEEVE CONFIGURATION, PERI-STRIPS STAPLE LINE REINFORCEMENT-STRIP CONFIGURATION	SYNOVIS SURGICAL INNOVATIONS
K040415	02/18/2004	PERI-STRIPS STAPLE LINE REINFORCEMENT - SLEEVE AND STRIP CONFIGURATIONS - AND PERI-STRIPS DRY STAPLE LINE REINFORCEMENT	SYNOVIS SURGICAL INNOVATIONS
K030879	03/20/2003	VERITAS COLLAGEN MATRIX	SYNOVIS SURGICAL INNOVATIONS
K062915	09/27/2006	VERITAS COLLAGEN MATRIX	SYNOVIS SURGICAL INNOVATIONS
K040001	01/02/2004	STEERABLE STYLET	SYNOVIS SURGICAL INNOVATIONS
K041669	06/21/2004	VERITAS DRY COLLAGEN MATRIX, VERITAS DRY OR VERITAS PSD	SYNOVIS SURGICAL INNOVATIONS
K122306	08/01/2012	SYNOVIS COLLAGEN MATRIX (TBD)	SYNOVIS SURGICAL INNOVATIONS
K083039	10/14/2008	VERITAS COLLAGEN MATRIX (DRY)	SYNOVIS SURGICAL INNOVATIONS