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Posterior Cervical Spine System

Page Type
Cleared 510(K)
510(k) Number
K233078
510(k) Type
Traditional
Applicant
Double Medical Technology, Inc.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/22/2023
Days to Decision
58 days
Submission Type
Summary

Posterior Cervical Spine System

Page Type
Cleared 510(K)
510(k) Number
K233078
510(k) Type
Traditional
Applicant
Double Medical Technology, Inc.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/22/2023
Days to Decision
58 days
Submission Type
Summary