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Solitaire 2 Revascularization Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162539
510(k) Type
Traditional
Applicant
MICRO THERAPEUTICS, INC. D/B/A EV3 NEUROVASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/2016
Days to Decision
59 days
Submission Type
Summary

Solitaire 2 Revascularization Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162539
510(k) Type
Traditional
Applicant
MICRO THERAPEUTICS, INC. D/B/A EV3 NEUROVASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/2016
Days to Decision
59 days
Submission Type
Summary