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COVIDIEN ENDO GIA RADIAL RELOAD WITH TRI-STAPLE TECHNOLOGY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102291
510(k) Type
Traditional
Applicant
COVIDIEN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/2010
Days to Decision
34 days
Submission Type
Summary

COVIDIEN ENDO GIA RADIAL RELOAD WITH TRI-STAPLE TECHNOLOGY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102291
510(k) Type
Traditional
Applicant
COVIDIEN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/2010
Days to Decision
34 days
Submission Type
Summary