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iFuse Implant System - iFuse Navigation

Page Type
Cleared 510(K)
PDF
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
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