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FLEXSTENT BILIARY SELF EXPANDING STENT SYSTEM MODEL FLX-DDLLL-BX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102519
510(k) Type
Traditional
Applicant
Flexible Stenting Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
11/22/2010
Days to Decision
81 days
Submission Type
Summary

FLEXSTENT BILIARY SELF EXPANDING STENT SYSTEM MODEL FLX-DDLLL-BX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102519
510(k) Type
Traditional
Applicant
Flexible Stenting Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
11/22/2010
Days to Decision
81 days
Submission Type
Summary