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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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