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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
FDA Hosted 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
FDA Hosted 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