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Versa-Fx Femoral Fixation System, Versa-Fx II Femoral Fixation System, Free-Lock Femoral Fixation System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150818
510(k) Type
Traditional
Applicant
Zimmer, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2015
Days to Decision
35 days
Submission Type
Summary

Versa-Fx Femoral Fixation System, Versa-Fx II Femoral Fixation System, Free-Lock Femoral Fixation System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150818
510(k) Type
Traditional
Applicant
Zimmer, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2015
Days to Decision
35 days
Submission Type
Summary