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Cervical Stand Alone System

Page Type
Cleared 510(K)
510(k) Number
K161280
510(k) Type
Special
Applicant
Orthofix Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2016
Days to Decision
42 days
Submission Type
Summary

Cervical Stand Alone System

Page Type
Cleared 510(K)
510(k) Number
K161280
510(k) Type
Special
Applicant
Orthofix Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2016
Days to Decision
42 days
Submission Type
Summary