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DIGITEX SUTURE DELIVERY SYSTEM, DIGITEXPOLYPROPYLENE SUTURE CARTRIDGE SIZE 0, WITH NEEDLE AND WITHOUT NEEDLE, DIGITEX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120284
510(k) Type
Traditional
Applicant
Coloplast A/S
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2012
Days to Decision
113 days
Submission Type
Summary

DIGITEX SUTURE DELIVERY SYSTEM, DIGITEXPOLYPROPYLENE SUTURE CARTRIDGE SIZE 0, WITH NEEDLE AND WITHOUT NEEDLE, DIGITEX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120284
510(k) Type
Traditional
Applicant
Coloplast A/S
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2012
Days to Decision
113 days
Submission Type
Summary