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DuoHex CH Cannulated Hammertoe System

Page Type
Cleared 510(K)
510(k) Number
K200840
510(k) Type
Traditional
Applicant
Nextremity Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/2020
Days to Decision
87 days
Submission Type
Summary

DuoHex CH Cannulated Hammertoe System

Page Type
Cleared 510(K)
510(k) Number
K200840
510(k) Type
Traditional
Applicant
Nextremity Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/2020
Days to Decision
87 days
Submission Type
Summary