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Cervical Plate System

Page Type
Cleared 510(K)
510(k) Number
K223753
510(k) Type
Traditional
Applicant
Double Medical Technology Inc.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
3/14/2023
Days to Decision
90 days
Submission Type
Summary

Cervical Plate System

Page Type
Cleared 510(K)
510(k) Number
K223753
510(k) Type
Traditional
Applicant
Double Medical Technology Inc.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
3/14/2023
Days to Decision
90 days
Submission Type
Summary