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FuseForce™ Flex Dynamic Compression System

Page Type
Cleared 510(K)
510(k) Number
K203832
510(k) Type
Traditional
Applicant
Wright Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/2021
Days to Decision
128 days
Submission Type
Summary

FuseForce™ Flex Dynamic Compression System

Page Type
Cleared 510(K)
510(k) Number
K203832
510(k) Type
Traditional
Applicant
Wright Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/2021
Days to Decision
128 days
Submission Type
Summary