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QUILL POLYPROPYLENE KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130078
510(k) Type
Traditional
Applicant
SURGICAL SPECIALTIES CORP. DBA ANGIOTECH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2013
Days to Decision
45 days
Submission Type
Summary

QUILL POLYPROPYLENE KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130078
510(k) Type
Traditional
Applicant
SURGICAL SPECIALTIES CORP. DBA ANGIOTECH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2013
Days to Decision
45 days
Submission Type
Summary