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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