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IdentiTi ALIF Interbody Systems

Page Type
Cleared 510(K)
510(k) Number
K232097
510(k) Type
Traditional
Applicant
Alphatec Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/2023
Days to Decision
74 days
Submission Type
Summary

IdentiTi ALIF Interbody Systems

Page Type
Cleared 510(K)
510(k) Number
K232097
510(k) Type
Traditional
Applicant
Alphatec Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/2023
Days to Decision
74 days
Submission Type
Summary