Last synced on 25 January 2026 at 3:41 am

Artix BG

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223000
510(k) Type
Traditional
Applicant
Inari Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/2023
Days to Decision
105 days
Submission Type
Summary

Artix BG

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223000
510(k) Type
Traditional
Applicant
Inari Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/2023
Days to Decision
105 days
Submission Type
Summary