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AZURE ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K130825
510(k) Type
Special
Applicant
ORTHOFIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/2013
Days to Decision
42 days
Submission Type
Summary

AZURE ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K130825
510(k) Type
Special
Applicant
ORTHOFIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/2013
Days to Decision
42 days
Submission Type
Summary