FDA 510(k) Applications Submitted by SURGICAL SPECIALTIES CORP. DBA ANGIOTECH

FDA 510(k) Number	Submission Date	Device Name	Applicant
K130078	01/14/2013	QUILL POLYPROPYLENE KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN	SURGICAL SPECIALTIES CORP. DBA ANGIOTECH
K122898	09/21/2012	QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN	SURGICAL SPECIALTIES CORP. DBA ANGIOTECH
K123409	11/05/2012	QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN	SURGICAL SPECIALTIES CORP. DBA ANGIOTECH
K133420	11/08/2013	TRANQUILL BARBED DEVICE	SURGICAL SPECIALTIES CORP. DBA ANGIOTECH
K123836	12/13/2012	QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN	SURGICAL SPECIALTIES CORP. DBA ANGIOTECH
K123877	12/17/2012	QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN	SURGICAL SPECIALTIES CORP. DBA ANGIOTECH
K131224	04/30/2013	SHARPOINT POLYPROPYLENE SURGICAL SUTURE, LOOK POLYPROPYLENE SURGICAL SUTURE, QUILL POLYPROPYLENE KNOTLESS TISSUE-CLOSURE	SURGICAL SPECIALTIES CORP. DBA ANGIOTECH