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Hercules Syndesmosis Implant System

Page Type
Cleared 510(K)
510(k) Number
K220260
510(k) Type
Traditional
Applicant
In2Bones USA, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2022
Days to Decision
59 days
Submission Type
Summary

Hercules Syndesmosis Implant System

Page Type
Cleared 510(K)
510(k) Number
K220260
510(k) Type
Traditional
Applicant
In2Bones USA, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2022
Days to Decision
59 days
Submission Type
Summary