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A-CIFT SoloFuse

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172484
510(k) Type
Traditional
Applicant
Spinefrontier, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2018
Days to Decision
264 days
Submission Type
Summary

A-CIFT SoloFuse

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172484
510(k) Type
Traditional
Applicant
Spinefrontier, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2018
Days to Decision
264 days
Submission Type
Summary