Surgical Specialties Corp. Dba Angiotech
Surgical Specialties Corp. Dba Angiotech holds FDA 510(k) medical device clearances, first cleared 2012, most recent 2013.
Top product codes for Surgical Specialties Corp. Dba Angiotech
Recent clearances by Surgical Specialties Corp. Dba Angiotech
- K133420 — TRANQUILL BARBED DEVICE
- K131224 — SHARPOINT POLYPROPYLENE SURGICAL SUTURE, LOOK POLYPROPYLENE SURGICAL SUTURE, QUILL POLYPROPYLENE KNOTLESS TISSUE-CLOSURE
- K130078 — QUILL POLYPROPYLENE KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN
- K123877 — QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN
- K123836 — QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN
- K123409 — QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN
- K122898 — QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN
Data sourced from openFDA. This site is unofficial and independent of the FDA.