Last synced on 23 September 2022 at 11:05 pm

Solitaire 4 Revascularization Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183022
510(k) Type
Traditional
Applicant
Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/2019
Days to Decision
89 days
Submission Type
Summary

Solitaire 4 Revascularization Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183022
510(k) Type
Traditional
Applicant
Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/2019
Days to Decision
89 days
Submission Type
Summary