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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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