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SI-BONE iFuse Implant System®

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193524
510(k) Type
Traditional
Applicant
Si-Bone, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2020
Days to Decision
103 days
Submission Type
Summary

SI-BONE iFuse Implant System®

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193524
510(k) Type
Traditional
Applicant
Si-Bone, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2020
Days to Decision
103 days
Submission Type
Summary