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MODIFIED ENDO STICH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082659
510(k) Type
Special
Applicant
COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2008
Days to Decision
7 days
Submission Type
Summary

MODIFIED ENDO STICH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082659
510(k) Type
Special
Applicant
COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2008
Days to Decision
7 days
Submission Type
Summary