FDA 510(k) Applications Submitted by ROBERT HOY

FDA 510(k) Number	Submission Date	Device Name	Applicant
K140970	04/16/2014	ONE-PIECE PEEK FUSION IMPLANT	MTP SOLUTIONS LLC
K171964	06/30/2017	LigaMetrics Suture Anchors	Mortise Medical LLC
K152236	08/10/2015	KATOR Suture Anchor	KATOR LLC
K162386	08/25/2016	KATOR Suture Anchor	KATOR LLC
K172620	08/31/2017	SyndesMetrics Syndesmosis Repair System	Mortise Medical LLC
K172943	09/26/2017	Flex-Thread Fibula Pin System	IntraFuse LLC
K173269	10/12/2017	KATOR Suture Anchor	KATOR LLC
K133229	10/21/2013	TITANIUM SUTURE ANCHOR	MTP SOLUTIONS LLC
K133235	10/21/2013	THREADED PEEK K-WIRE	MTP SOLUTIONS LLC
K133515	11/15/2013	PEEK FUSION IMPLANT	MTP SOLUTIONS LLC
K163440	12/08/2016	Stealth Staple System	FIRST RAY LLC
K163488	12/12/2016	Flex-Thread Clavicle Pin System	INTRAFUSE LLC
K153585	12/16/2015	Flip Button Suture Anchor	FIRST RAY LLC
K153622	12/18/2015	First Ray Internal Bone Staple System	FIRST RAY LLC
K153638	12/18/2015	Bicortical Fixation Screw & Washer Nut System	FIRST RAY LLC