FDA 510(k) Applications Submitted by Gregory Foster

FDA 510(k) Number	Submission Date	Device Name	Applicant
K200209	01/28/2020	Persona Personalized Knee System	Zimmer, Inc.
K240299	02/01/2024	Persona the Personalized Knee System (Persona OsseoTi 3-Peg Patella)	Zimmer, Inc.
K230321	02/06/2023	PersonaÖ Personalized Knee System	Zimmer, Inc.
K221479	05/23/2022	Persona Personalized Knee System	Zimmer, Inc.
K212431	08/04/2021	Biomet Answer/Impact/Integral Distal Centralizer/Centering Sleeve	Biomet, Inc.
K242543	08/26/2024	Persona the Personalized Knee System (Persona Ti-Nidium PPS Femurs)	Zimmer, Inc.
K243247	10/11/2024	Persona the Personalized Knee System	Zimmer, Inc.
K193223	11/22/2019	Persona Personalized Knee System	Zimmer, Inc
K243724	12/03/2024	Persona« Revision Knee System (Persona Revision SoluTionÖ Femoral Components)	Zimmer, Inc.