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Connector System

Page Type
Cleared 510(K)
510(k) Number
K190751
510(k) Type
Traditional
Applicant
Orthofix Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2019
Days to Decision
58 days
Submission Type
Summary

Connector System

Page Type
Cleared 510(K)
510(k) Number
K190751
510(k) Type
Traditional
Applicant
Orthofix Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2019
Days to Decision
58 days
Submission Type
Summary