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SYNTHES (USA) TOMOFIX MEDIAL DISTAL FEMUR PLATES

Page Type
Cleared 510(K)
510(k) Number
K081353
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2008
Days to Decision
70 days
Submission Type
Summary

SYNTHES (USA) TOMOFIX MEDIAL DISTAL FEMUR PLATES

Page Type
Cleared 510(K)
510(k) Number
K081353
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2008
Days to Decision
70 days
Submission Type
Summary