FDA 510(k) Applications Submitted by FOSTER BOOP

FDA 510(k) Number Submission Date Device Name Applicant
K010073 01/09/2001 SPLINE DENTAL IMPLANT SYSTEM SULZER CALCITEK, INC.
K110335 02/04/2011 CERAMIC BRACKETS ORTHO ORGANIZERS, INC.
K011245 04/23/2001 ADVENT IMPLANT SYSTEM, SWISS PLUS IMPLANT SYSTEM SULZER DENTAL, INC.
K981562 05/01/1998 SPLINE DENTAL IMPLANT SYSTEM - SPLINE XI IMPLANT SULZER CALCITEK, INC.
K001786 06/13/2000 TEMPORARY GINGIVAL CUFF AND IMPRESSION POST AND IMPLANT ANALOG SULZER CALCITEK, INC.
K982305 07/01/1998 SPLINE DENTAL IMPLANT SYSTEM-TEMPORARY ABUTMENT SULZER CALCITEK, INC.
K012055 07/02/2001 3.25MM SPLINE TWIST IMPLANT SULZER DENTAL, INC.
K051993 07/25/2005 LMA FASTRACH ETT SINGLE USE THE LARYNGEAL MASK CO.,LTD.
K062475 08/24/2006 LMA STONEBREAKER DEVICE; PROBE SIZE 1.0MM, 1.6MM, 2.0MM THE LARYNGEAL MASK CO.,LTD.
K973521 09/17/1997 VARIABLE PARALLEL PIN SULZER CALCITEK, INC.
K013227 09/27/2001 SCREW VENT IMPLANT; TAPERED SCREW VENT IMPLANT SULZER DENTAL, INC.
K013494 10/22/2001 3.75MM AND 5.0MM SPLINE TWIST IMPLANT SULZER DENTAL, INC.
K974392 11/21/1997 LEADFIX BIORESORBABLE MEMBRANCE PIN SYSTEM BIOVISION GMBH
K984536 12/21/1998 REMOVABLE CUFF ABUTMENT SULZER CALCITEK, INC.


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