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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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