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Akros Fibulink Syndesmosis Repair Kit

Page Type
Cleared 510(K)
510(k) Number
K162805
510(k) Type
Traditional
Applicant
Akros Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2017
Days to Decision
97 days
Submission Type
Summary

Akros Fibulink Syndesmosis Repair Kit

Page Type
Cleared 510(K)
510(k) Number
K162805
510(k) Type
Traditional
Applicant
Akros Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2017
Days to Decision
97 days
Submission Type
Summary