FDA 510(k) Applications Submitted by Smith & Nephew, Inc

FDA 510(k) Number	Submission Date	Device Name	Applicant
K170282	01/30/2017	Smith & Nephew VISIONAIRE Adaptive Guides	Smith & Nephew, Inc
K082211	08/06/2008	RENASYS-F NEGATIVE PRESSURE WOUND THERAPY FOAM DRESSING KITS	Smith & Nephew, Inc
K142520	09/08/2014	Smith & Nephew, Inc. Spatialframe.com V5.0 Web-based software	Smith & Nephew, Inc
K200227	01/30/2020	Journey II XR Knee Instrument	Smith & Nephew, Inc
K190253	02/07/2019	EVOS Small Fragment Upper Extremity Plates Line Additions	Smith & Nephew, Inc
K103793	12/27/2010	DURAFIBER AG	Smith & Nephew, Inc
K140879	04/07/2014	BIOSURE HEALICOIL PK INTERFERENCE SCREW	Smith & Nephew, Inc
K142948	10/10/2014	BIOSURE REGENESORB interference Screw	Smith & Nephew, Inc