ClearanceBrief
Company ยท US

Surgical Specialties Corp. Dba Angiotech

FDA 510(k) clearances and medical device recalls filed under this name, 2012 to 2013. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GAMSuture, Absorbable, Synthetic, Polyglycolic Acid3
NEWSuture, Surgical, Absorbable, Polydioxanone3
GAWSuture, Nonabsorbable, Synthetic, Polypropylene2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 29, 2013K133420TRANQUILL BARBED DEVICE
Surgical Specialties Corp. Dba Angiotech
NEW
Aug 23, 2013K132268QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN
Surgical Specialties Corporation Dba Angiotech
NEW
May 16, 2013K131224SHARPOINT POLYPROPYLENE SURGICAL SUTURE, LOOK POLYPROPYLENE SURGICAL SUTURE, QUILL POLYPROPYLENE KNOTLESS TISSUE-CLOSURE
Surgical Specialties Corp. Dba Angiotech
GAW
Feb 28, 2013K130078QUILL POLYPROPYLENE KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN
Surgical Specialties Corp. Dba Angiotech
GAW
Jan 2, 2013K123877QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN
Surgical Specialties Corp. Dba Angiotech
NEW
Dec 21, 2012K123836QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN
Surgical Specialties Corp. Dba Angiotech
GAM
Nov 20, 2012K123409QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN
Surgical Specialties Corp. Dba Angiotech
GAM
Oct 22, 2012K122898QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN
Surgical Specialties Corp. Dba Angiotech
GAM

Latest recalls

DateFirm and productCodeLinked 510(k)
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