FDA 510(k) Applications Submitted by Jessica Staub

FDA 510(k) Number Submission Date Device Name Applicant
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.
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.


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