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FuzeFix Screw System

Page Type
Cleared 510(K)
510(k) Number
K170038
510(k) Type
Traditional
Applicant
Fusion Orthopedics, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/2017
Days to Decision
214 days
Submission Type
Summary

FuzeFix Screw System

Page Type
Cleared 510(K)
510(k) Number
K170038
510(k) Type
Traditional
Applicant
Fusion Orthopedics, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/2017
Days to Decision
214 days
Submission Type
Summary