FDA 510(k) Applications Submitted by ALTATEC GMBH

FDA 510(k) Number	Submission Date	Device Name	Applicant
K160784	03/22/2016	CAM Titanium Blanks	ALTATEC GMBH
K151599	06/12/2015	iSy Implant System	Altatec GmbH
K152509	09/02/2015	CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)	ALTATEC GMBH
K153779	12/31/2015	Abutment for Bridges	ALTATEC GmbH
K143337	11/20/2014	CONELOG Titanium base CAD/CAM	ALTATEC GMBH
K071213	05/01/2007	CAMLOG LOGFIT PROSTHETIC SYSTEM	ALTATEC GMBH
K090347	02/11/2009	CAMLOG ABUTMENTS PS	ALTATEC GMBH
K103252	11/03/2010	CAMLOG VARIO SR ABUTMENTS	ALTATEC GMBH
K113779	12/22/2011	CONELOG IMPLANT SYSTEM	ALTATEC GMBH
K133991	12/26/2013	ISY	ALTATEC GMBH
K083496	11/25/2008	CAMLOG IMPLANT SYSTEM MODIFIED IMPLANTS AND ABUTMENTS	ALTATEC GMBH
K073553	12/18/2007	CAMLOG IMPLANT SYSTEM ABUTMENTS	ALTATEC GMBH
K193401	12/06/2019	Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants	Altatec GmbH
K051636	06/20/2005	CAMLOG DENTAL IMPLANT ABUTMENTS, HEALING CAPS, AND ACCESSORIES	ALTATEC GMBH