FDA 510(k) Applications Submitted by Brock Johnson

FDA 510(k) Number	Submission Date	Device Name	Applicant
K230204	01/25/2023	ALPHALOK Plating System	Vilex LLC
K230462	02/21/2023	OPTIX H2 Patient Specific Instrument System	Vilex, LLC
K231493	05/23/2023	NITINEX Memory Compression Staple	Vilex, LLC
K231504	05/24/2023	TITANEXÖ MICROBEAM Screw System, TITANEXÖ ARTEMIS Screw System	Vilex LLC
K221558	05/31/2022	ALPHALOK Plating System	Vilex LLC
K122936	09/24/2012	ANKLE TRAUMA SYSTEM	ORTHOPRO LLC