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Cannulated Compression Device System

Page Type
Cleared 510(K)
510(k) Number
K210146
510(k) Type
Traditional
Applicant
Orthopedic Designs North America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2022
Days to Decision
447 days
Submission Type
Summary

Cannulated Compression Device System

Page Type
Cleared 510(K)
510(k) Number
K210146
510(k) Type
Traditional
Applicant
Orthopedic Designs North America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2022
Days to Decision
447 days
Submission Type
Summary