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IdentiTi™ II Interbody System

Page Type
Cleared 510(K)
510(k) Number
K242364
510(k) Type
Traditional
Applicant
Alphatec Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/2024
Days to Decision
56 days
Submission Type
Summary

IdentiTi™ II Interbody System

Page Type
Cleared 510(K)
510(k) Number
K242364
510(k) Type
Traditional
Applicant
Alphatec Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/2024
Days to Decision
56 days
Submission Type
Summary