FDA 510(k) Applications Submitted by ALPHATEC SPINE

FDA 510(k) Number Submission Date Device Name Applicant
K160958 04/05/2016 Battalion Universal Spacer System ALPHATEC SPINE
K222028 07/11/2022 IdentiTiÖ Porous Ti Interbody System, IdentiTiÖ NanoTecÖ Interbody System, TranscendÖ PEEK Interbody System, TranscendÖ NanoTecÖ Interbody System, IdentiTiÖ ALIF Standalone Interbody System, IdentiTiÖ NanoTecÖ ALIF Standalone Interbody System Alphatec Spine
K191185 05/03/2019 Solanas« Posterior OCT Fixation System Alphatec Spine


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