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SYNTHES (USA) MEDIAL DISTAL TIBIA PLATES

Page Type
Cleared 510(K)
510(k) Number
K001945
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/2000
Days to Decision
88 days
Submission Type
Summary

SYNTHES (USA) MEDIAL DISTAL TIBIA PLATES

Page Type
Cleared 510(K)
510(k) Number
K001945
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/2000
Days to Decision
88 days
Submission Type
Summary