Last synced on 25 April 2025 at 11:05 pm

Artix Thrombectomy Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220600
510(k) Type
Special
Applicant
Inari Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/2022
Days to Decision
23 days
Submission Type
Summary

Artix Thrombectomy Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220600
510(k) Type
Special
Applicant
Inari Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/2022
Days to Decision
23 days
Submission Type
Summary