FDA 510(k) Applications Submitted by Jessica Staub

FDA 510(k) Number	Submission Date	Device Name	Applicant
K250554	02/25/2025	prodisc« L Instruments	Centinel Spine LLC
K221848	06/24/2022	prodisc C SK, prodisc C Nova, and prodisc C Vivo Instruments	Centinel Spine LLC
K152211	08/07/2015	PCT System	CENTINEL SPINE, INC.
K242869	09/20/2024	prodisc« L Instruments	Centinel Spine LLC
K173347	10/25/2017	STALIF C FLX, STALIF M FLX, STALIF L FLX and STALIF Lateral-Oblique FLX, ACTILIF C FLX, ACTILIF M FLX, ACTILIF L FLX and ACTILIF Lateral-Oblique FLX	Centinel Spine, Inc.