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A-CIFT SoloFuse

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151198
510(k) Type
Special
Applicant
SPINEFRONTIER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/2015
Days to Decision
73 days
Submission Type
Summary

A-CIFT SoloFuse

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151198
510(k) Type
Special
Applicant
SPINEFRONTIER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/2015
Days to Decision
73 days
Submission Type
Summary