Last synced on 22 September 2023 at 11:04 pm

QUILL MONODERM 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
K123409
510(k) Type
Traditional
Applicant
SURGICAL SPECIALTIES CORP. DBA ANGIOTECH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2012
Days to Decision
15 days
Submission Type
Summary

QUILL MONODERM 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
K123409
510(k) Type
Traditional
Applicant
SURGICAL SPECIALTIES CORP. DBA ANGIOTECH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2012
Days to Decision
15 days
Submission Type
Summary