Last synced on 14 November 2025 at 11:06 pm

KITE Distal Fibula Kit

Page Type
Cleared 510(K)
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)
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