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Calibrate LTX Interbody System

Page Type
Cleared 510(K)
510(k) Number
K223611
510(k) Type
Traditional
Applicant
Alphatec Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/2023
Days to Decision
117 days
Submission Type
Summary

Calibrate LTX Interbody System

Page Type
Cleared 510(K)
510(k) Number
K223611
510(k) Type
Traditional
Applicant
Alphatec Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/2023
Days to Decision
117 days
Submission Type
Summary