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GENTAFIX® (1, 3, 3MV)

Page Type
Cleared 510(K)
510(k) Number
K242216
510(k) Type
Traditional
Applicant
Teknimed SAS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
12/18/2024
Days to Decision
142 days
Submission Type
Summary

GENTAFIX® (1, 3, 3MV)

Page Type
Cleared 510(K)
510(k) Number
K242216
510(k) Type
Traditional
Applicant
Teknimed SAS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
12/18/2024
Days to Decision
142 days
Submission Type
Summary