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PROFEMUR XM DISTAL CENTRALIZER

Page Type
Cleared 510(K)
510(k) Number
K130167
510(k) Type
Traditional
Applicant
WRIGHT MEDICAL TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2013
Days to Decision
86 days
Submission Type
Summary

PROFEMUR XM DISTAL CENTRALIZER

Page Type
Cleared 510(K)
510(k) Number
K130167
510(k) Type
Traditional
Applicant
WRIGHT MEDICAL TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2013
Days to Decision
86 days
Submission Type
Summary