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Connector System

Page Type
Cleared 510(K)
510(k) Number
K170647
510(k) Type
Traditional
Applicant
Orthofix Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/2017
Days to Decision
69 days
Submission Type
Summary

Connector System

Page Type
Cleared 510(K)
510(k) Number
K170647
510(k) Type
Traditional
Applicant
Orthofix Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/2017
Days to Decision
69 days
Submission Type
Summary