FDA 510(k) Applications Submitted by Alphatec Spine

FDA 510(k) Number	Submission Date	Device Name	Applicant
K240951	04/08/2024	Invictus Robotic Navigation Instruments	Alphatec Spine
K241375	05/15/2024	IdentiTi Porous Ti Interbody System; IdentiTi NanoTec Interbody System; IdentiTi Cervical Porous Ti Interbody System; IdentiTi NanoTec Cervical Interbody System; IdentiTi Cervical Standalone Interbody System; IdentiTi NanoTec Cervical Standalone Interbody	Alphatec Spine
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