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ORTHOLOC® 3Di Foot Plating Reconstruction System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152974
510(k) Type
Traditional
Applicant
Wrightmedicaltechnologyinc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2015
Days to Decision
64 days
Submission Type
Summary

ORTHOLOC® 3Di Foot Plating Reconstruction System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152974
510(k) Type
Traditional
Applicant
Wrightmedicaltechnologyinc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2015
Days to Decision
64 days
Submission Type
Summary