Last synced on 14 November 2025 at 11:06 pm

Artix Thrombectomy Device

Page Type
Cleared 510(K)
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)
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