Last synced on 2 May 2025 at 11:05 pm

iFuse Implant System - iFuse Navigation

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203110
510(k) Type
Special
Applicant
SI-BONE, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/2020
Days to Decision
25 days
Submission Type
Summary

iFuse Implant System - iFuse Navigation

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203110
510(k) Type
Special
Applicant
SI-BONE, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/2020
Days to Decision
25 days
Submission Type
Summary