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iFuse-TORQ™ Implant System

Page Type
Cleared 510(K)
510(k) Number
K203247
510(k) Type
Traditional
Applicant
Si-Bone, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2021
Days to Decision
113 days
Submission Type
Summary

iFuse-TORQ™ Implant System

Page Type
Cleared 510(K)
510(k) Number
K203247
510(k) Type
Traditional
Applicant
Si-Bone, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2021
Days to Decision
113 days
Submission Type
Summary