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FDA 510(k) Applications Submitted by Alphatec Spine Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K222973
09/28/2022
IdentiTi and Transcend Interbody Systems: IndentiTi Cervical Porous Ti Interbody System, IdentiTi NanoTec Cervical Interbody System, Transcend Cervical PEEK Interbody System, Transcend NanoTec Cervical Interbody System, IdentiTi Cervical Standalone Interb
Alphatec Spine Inc.
K203742
12/22/2020
IdentiTi ALIF Standalone Interbody System
Alphatec Spine Inc.
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