Last synced on 25 January 2026 at 3:41 am

iFuse TORQ® Implant System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222605
510(k) Type
Special
Applicant
Si-Bone, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2022
Days to Decision
31 days
Submission Type
Summary

iFuse TORQ® Implant System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222605
510(k) Type
Special
Applicant
Si-Bone, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2022
Days to Decision
31 days
Submission Type
Summary