K-number	K113744
Device name	QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIOXANONE)
Applicant	Angiotech
Product code	NEW
Device class	Class II
Decision date	Feb 1, 2012
Decision	Substantially Equivalent
Regulation	878.4840

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View the full FDA submission: accessdata.fda.gov

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QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIOXANONE)

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