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Akros Scruture Anchor LisFranc Repair Kit

Page Type
Cleared 510(K)
510(k) Number
K200361
510(k) Type
Traditional
Applicant
Akros Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/2020
Days to Decision
52 days
Submission Type
Summary

Akros Scruture Anchor LisFranc Repair Kit

Page Type
Cleared 510(K)
510(k) Number
K200361
510(k) Type
Traditional
Applicant
Akros Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/2020
Days to Decision
52 days
Submission Type
Summary