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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