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VARIAX DISTAL FIBULA PLATE

Page Type
Cleared 510(K)
510(k) Number
K081284
510(k) Type
Traditional
Applicant
HOWMEDICA OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/2008
Days to Decision
73 days
Submission Type
Summary

VARIAX DISTAL FIBULA PLATE

Page Type
Cleared 510(K)
510(k) Number
K081284
510(k) Type
Traditional
Applicant
HOWMEDICA OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/2008
Days to Decision
73 days
Submission Type
Summary