FDA 510(k) Applications Submitted by Cynthia Dorne

FDA 510(k) Number Submission Date Device Name Applicant
K211873 06/17/2021 PSX Interbody System Alphatec Spine, Inc.
K232275 07/31/2023 Invictus« Spinal Fixation System Alphatec Spine, Inc.
K222455 08/15/2022 Calibrate LTX Interbody System Alphatec Spine, Inc.
K203056 10/08/2020 InvictusÖ Spinal Fixation System Alphatec Spine, Inc.
K203742 12/22/2020 IdentiTi ALIF Standalone Interbody System Alphatec Spine Inc.


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