FDA 510(k) Applications Submitted by KATI MARTTINEN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K090177	01/23/2009	INION BIORESTORE BIODEGRADABLE BONE GRAFT SUBSTITUTE	INION OY
K070998	04/09/2007	INION BIORESTORE	INION OY
K151360	05/20/2015	Inion Spinal Graft Containment System	Inion Oy
K071464	05/29/2007	INION HEXALON BIODEGRADABLE ACL/PCL SCREW	INION OY
K071810	07/02/2007	INION SPINAL GRAFT CONTAINMENT SYSTEM	INION LTD.
K062782	09/18/2006	INION ANCHRON PLUS BIODEGRADABLE ANCHOR SYSTEM, MODEL ANC-6001	INION OY
K122890	09/20/2012	INION CPS ORBITAL PLATES	INION OY
K203105	10/15/2020	Inion CompressOn Screw	Inion Oy
K063410	11/13/2006	INION CPS/OTPS FREEDOMPLATE	INION LTD.
K123672	11/29/2012	INION FREEDOMSCREW (ALTERNATIVE MARKETING NAME: INION OTPS FREEDOMSCREW)	INION OY
K133932	12/23/2013	INION FREEDOMPIN	INION OY