FDA 510(k) Applications Submitted by Jeremy Clark

FDA 510(k) Number	Submission Date	Device Name	Applicant
K240175	01/23/2024	Tigon Medical Fractures, Instability, and Reconstruction (FIRE)	Tigon Medical
K230311	02/03/2023	HyperSuture	Threadstone L.L.C.
K220464	02/17/2022	Tigon Medical Gryphon Anchor Line	Tigon Medical
K211049	04/08/2021	Tigon Medical Button System	Tigon Medical
K241376	05/15/2024	HyperSuture All Blue Extension Line	Threadstone L.L.C.
K242201	07/26/2024	HyperSuture White/Green Extension Line	Threadstone LLC
K242529	08/26/2024	Tigon Medical All-Suture Anchors (ASA)	Tigon Medical
K182507	09/12/2018	Tigon Medical Tissue Anchors	Tigon Medical
K234079	12/22/2023	HyperSuture Extension Line	Threadstone L.L.C.