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SOLITAIRE 2 REVASCULARIZATION DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141491
510(k) Type
Traditional
Applicant
Micro Therapeutics Inc., d/b/a ev3 Neurovascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2014
Days to Decision
139 days
Submission Type
Summary

SOLITAIRE 2 REVASCULARIZATION DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141491
510(k) Type
Traditional
Applicant
Micro Therapeutics Inc., d/b/a ev3 Neurovascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2014
Days to Decision
139 days
Submission Type
Summary