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Hand Trauma Screw System

Page Type
Cleared 510(K)
510(k) Number
K220723
510(k) Type
Traditional
Applicant
Skeletal Dynamics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/2022
Days to Decision
59 days
Submission Type
Summary

Hand Trauma Screw System

Page Type
Cleared 510(K)
510(k) Number
K220723
510(k) Type
Traditional
Applicant
Skeletal Dynamics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/2022
Days to Decision
59 days
Submission Type
Summary