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IdentiTi Porous Ti Interbody System

Page Type
Cleared 510(K)
510(k) Number
K183705
510(k) Type
Traditional
Applicant
Alphatec Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2019
Days to Decision
60 days
Submission Type
Summary

IdentiTi Porous Ti Interbody System

Page Type
Cleared 510(K)
510(k) Number
K183705
510(k) Type
Traditional
Applicant
Alphatec Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2019
Days to Decision
60 days
Submission Type
Summary