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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
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