FDA 510(k) Applications Submitted by Sharyn Orton

FDA 510(k) Number	Submission Date	Device Name	Applicant
K140106	01/15/2014	S128 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM	Renovis Surgical Technologies, Inc.
K131354	05/10/2013	RENOVIS BIPOLAR HIP SYSTEM	RENOVIS SURGICAL TECHNOLOGIES LLC
K141370	05/27/2014	RENOVIS CEMENTED HIP SYSTEM	Renovis Surgical Technologies, Inc.
K131766	06/17/2013	PLATINUM DRF IMAGING SYSTEM	APELEM-DMS GROUP
K142095	08/01/2014	RENOVIS S134 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM	Renovis Surgical Technologies, Inc.
K122850	09/18/2012	TALOS-C CERVICAL INTERVERTEBRAL BODY FUSION DEVICES	MEDITECH ADVISORS, LLC
K123829	12/12/2012	PORTABLE THERAPEUTIX SQUID ACTIVE COLD COMPRESSION DEVICE AND COLD PACK	PORTABLE THERAPEUTIX, LLC
K131122	04/22/2013	S128 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM	RENOVIS SURGICAL TECHNOLOGIES, LLC
K141676	06/23/2014	RENOVIS SURGICAL POROUS ACETABULAR CUP SYSTEM	Renovis Surgical Technologies, Inc.
K132312	07/25/2013	RENOVIS TESERA TRABECULAR TECHNOLOGY (T3) ACETABULAR SHELL SYSTEM	RENOVIS SURGICAL TECHNOLOGIES, LLC
K133483	11/13/2013	PORTABLE THERAPEUTIX SQUID ACTIVE COLD COMPRESSION DEVICE AND COLD PACK FOR OTC USE	PORTABLE THERAPEUTIX
K110462	02/17/2011	KEPLER MEDTEC DISPOSABLE BIPOLAR CABLE	KEPLER MEDTEC