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Calibrate LTX Interbody System

Page Type
Cleared 510(K)
510(k) Number
K222455
510(k) Type
Traditional
Applicant
Alphatec Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/2022
Days to Decision
95 days
Submission Type
Summary

Calibrate LTX Interbody System

Page Type
Cleared 510(K)
510(k) Number
K222455
510(k) Type
Traditional
Applicant
Alphatec Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/2022
Days to Decision
95 days
Submission Type
Summary