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CONSTRUX MINI PEEK SPACER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K101812
510(k) Type
Traditional
Applicant
ORTHOFIX INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/2010
Days to Decision
90 days
Submission Type
Summary

CONSTRUX MINI PEEK SPACER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K101812
510(k) Type
Traditional
Applicant
ORTHOFIX INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/2010
Days to Decision
90 days
Submission Type
Summary