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Calibrate CCX Interbody System

Page Type
Cleared 510(K)
510(k) Number
K232504
510(k) Type
Traditional
Applicant
Alphatec Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/13/2023
Days to Decision
56 days
Submission Type
Summary

Calibrate CCX Interbody System

Page Type
Cleared 510(K)
510(k) Number
K232504
510(k) Type
Traditional
Applicant
Alphatec Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/13/2023
Days to Decision
56 days
Submission Type
Summary