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SpineFrontier SIJFuse Sacroiliac Joint Fusion Device System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150017
510(k) Type
Traditional
Applicant
SpineFrontier, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/2015
Days to Decision
109 days
Submission Type
Summary

SpineFrontier SIJFuse Sacroiliac Joint Fusion Device System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150017
510(k) Type
Traditional
Applicant
SpineFrontier, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/2015
Days to Decision
109 days
Submission Type
Summary