FDA 510(k) Applications Submitted by Neha Mohindroo

FDA 510(k) Number Submission Date Device Name Applicant
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
K223611 12/02/2022 Calibrate LTX Interbody System Alphatec Spine, Inc.


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