Last synced on 4 July 2025 at 11:05 pm

QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIOXANONE)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113744
510(k) Type
Traditional
Applicant
ANGIOTECH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/2012
Days to Decision
43 days
Submission Type
Summary

QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIOXANONE)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113744
510(k) Type
Traditional
Applicant
ANGIOTECH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/2012
Days to Decision
43 days
Submission Type
Summary