FDA 510(k) Applications Submitted by restor3d

FDA 510(k) Number	Submission Date	Device Name	Applicant
K231458	05/19/2023	Extremity Staple	restor3d
K234087	12/22/2023	restor3d TIDAL Lumbar Interbody Fusion System	restor3d
K241482	05/24/2024	Kinos Total Ankle System	restor3d
K232595	08/25/2023	Kinos Axiom Total Ankle System	restor3d
K242868	09/20/2024	Kinos Total Ankle System	restor3d
K223326	10/31/2022	Axiom PSR System	Restor3d
K243643	11/26/2024	restor3d Reverse Total Shoulder Arthroplasty System	restor3d
K211789	06/10/2021	restor3d Pin Implants	restor3d
K193491	12/17/2019	restor3d Metallic Interference Screw	restor3D
K220523	02/23/2022	restor3d TiDAL Lumbar Interbody Fusion Device	Restor3d