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DynaFuse Fixation System

Page Type
Cleared 510(K)
510(k) Number
K203595
510(k) Type
Traditional
Applicant
MedShape, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/2022
Days to Decision
391 days
Submission Type
Summary

DynaFuse Fixation System

Page Type
Cleared 510(K)
510(k) Number
K203595
510(k) Type
Traditional
Applicant
MedShape, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/2022
Days to Decision
391 days
Submission Type
Summary