Last synced on 23 September 2022 at 11:05 pm

Solitaire Platinum Revascularization Device, Solitaire X Revascularization Device (Solitaire Revascularization Device)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193576
510(k) Type
Traditional
Applicant
Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2020
Days to Decision
333 days
Submission Type
Summary

Solitaire Platinum Revascularization Device, Solitaire X Revascularization Device (Solitaire Revascularization Device)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193576
510(k) Type
Traditional
Applicant
Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2020
Days to Decision
333 days
Submission Type
Summary