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SINEXUS SINUS STENT GEN 2, MODEL 1999-25

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092401
510(k) Type
Traditional
Applicant
SINEXUS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2009
Days to Decision
103 days
Submission Type
Summary

SINEXUS SINUS STENT GEN 2, MODEL 1999-25

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092401
510(k) Type
Traditional
Applicant
SINEXUS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2009
Days to Decision
103 days
Submission Type
Summary