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iFUSE Implant System

Page Type
Cleared 510(K)
510(k) Number
K160652
510(k) Type
Traditional
Applicant
SI-BONE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2016
Days to Decision
87 days
Submission Type
Summary

iFUSE Implant System

Page Type
Cleared 510(K)
510(k) Number
K160652
510(k) Type
Traditional
Applicant
SI-BONE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2016
Days to Decision
87 days
Submission Type
Summary