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KITE Distal Fibula Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230623
510(k) Type
Traditional
Applicant
Intrauma S.p.A
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
9/1/2023
Days to Decision
179 days
Submission Type
Summary

KITE Distal Fibula Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230623
510(k) Type
Traditional
Applicant
Intrauma S.p.A
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
9/1/2023
Days to Decision
179 days
Submission Type
Summary