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Centurion POCT System

Page Type
Cleared 510(K)
510(k) Number
K150822
510(k) Type
Traditional
Applicant
ORTHOFIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2015
Days to Decision
49 days
Submission Type
Summary

Centurion POCT System

Page Type
Cleared 510(K)
510(k) Number
K150822
510(k) Type
Traditional
Applicant
ORTHOFIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2015
Days to Decision
49 days
Submission Type
Summary