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Solitare Platinum Revascularization Device

Page Type
Cleared 510(K)
510(k) Number
K181186
510(k) Type
Traditional
Applicant
Micro Therapeutics Inc. D/B/A Ev3 Neurovascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/2018
Days to Decision
175 days
Submission Type
Summary

Solitare Platinum Revascularization Device

Page Type
Cleared 510(K)
510(k) Number
K181186
510(k) Type
Traditional
Applicant
Micro Therapeutics Inc. D/B/A Ev3 Neurovascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/2018
Days to Decision
175 days
Submission Type
Summary