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OSTIAL PRO STENT POSITIONING SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062192
510(k) Type
Traditional
Applicant
Ostial Solutions, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/24/2007
Days to Decision
297 days
Submission Type
Summary

OSTIAL PRO STENT POSITIONING SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062192
510(k) Type
Traditional
Applicant
Ostial Solutions, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/24/2007
Days to Decision
297 days
Submission Type
Summary