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CONSTRUX MINI PEEK; SPACER SYSTEM, TI SPACER SYSTEM, CERVICAL STAND ALONE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142152
510(k) Type
Traditional
Applicant
ORTHOFIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/2015
Days to Decision
155 days
Submission Type
Summary

CONSTRUX MINI PEEK; SPACER SYSTEM, TI SPACER SYSTEM, CERVICAL STAND ALONE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142152
510(k) Type
Traditional
Applicant
ORTHOFIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/2015
Days to Decision
155 days
Submission Type
Summary