FDA 510(k) Applications Submitted by KLS MARTIN L.P.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K220050	01/06/2022	KLS Martin IPS Distraction	KLS Martin L.P.
K070169	01/18/2007	KLS MARTIN QUICK DISC, STERNAL TALON AND STERNAL PLATING - STERILE	KLS MARTIN L.P.
K060177	01/23/2006	KLS MARTIN RIGID FIXATION - STERILE	KLS MARTIN L.P.
K150771	03/24/2015	RxG Distraction System	KLS MARTIN L.P.
K151382	05/22/2015	Patient Contoured Implant-PEEK (PCI-PEEK)	KLS MARTIN L.P.
K141489	06/05/2014	LINOS MOH HAND PLATING SYSTEM	KLS MARTIN L.P.
K151983	07/17/2015	KLS Martin LSS Plating System	KLS MARTIN L.P.
K122860	09/18/2012	KLS MARTIN RECON TALON	KLS MARTIN L.P.
K062857	09/25/2006	KLS MARTIN QUICK DISC	KLS MARTIN L.P.
K221938	07/01/2022	KLS Martin Pure Pectus System	KLS Martin L.P.
K083432	11/20/2008	DRILL FREE MMF SCREW	KLS MARTIN L.P.
K072764	09/28/2007	KLS MARTIN XTERNAL FIXATOR	KLS MARTIN L.P.