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Solitaire 2 and Solitaire Platinum Revascularization Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181060
510(k) Type
Traditional
Applicant
Medtronic Neurovascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2018
Days to Decision
123 days
Submission Type
Summary

Solitaire 2 and Solitaire Platinum Revascularization Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181060
510(k) Type
Traditional
Applicant
Medtronic Neurovascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2018
Days to Decision
123 days
Submission Type
Summary