Last synced on 25 January 2026 at 3:41 am

xvision Spine System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220905
510(k) Type
Traditional
Applicant
Augmedics, Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
11/17/2022
Days to Decision
234 days
Submission Type
Summary

xvision Spine System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220905
510(k) Type
Traditional
Applicant
Augmedics, Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
11/17/2022
Days to Decision
234 days
Submission Type
Summary