FDA 510(k) Applications Submitted by WINSTON D GREER

FDA 510(k) Number Submission Date Device Name Applicant
K980374 01/30/1998 IMPLANT SITE DILATORS BIOHORIZONS IMPLANT SYSTEMS, INC.
K030463 02/12/2003 MODIFICATION TO THE MAESTRO SYSTEM BIOHORIZONS IMPLANT SYSTEMS, INC.
K061567 06/06/2006 BIOHORIZONS CERAMIC ABUTMENT BIOHORIZONS IMPLANT SYSTEMS, INC.
K041938 07/19/2004 MAXIMUS OS (OVERDENTURE SYSTEM) BIOHORIZONS IMPLANT SYSTEMS, INC.
K022790 08/22/2002 THE AUTOTAC SYSTEM TITANIUM TACK BIOHORIZONS IMPLANT SYSTEMS, INC.
K022795 08/23/2002 MODIFICATION TO THE MAESTRO SYSTEM BIOHORIZONS IMPLANT SYSTEMS, INC.
K052419 09/02/2005 MAXIMUS 3.0 AND OS IMPLANTS BIOHORIZONS IMPLANT SYSTEMS, INC.
K042429 09/08/2004 THE PRODIGY SYSTEM DENTAL IMPLANTS BIOHORIZONS IMPLANT SYSTEMS, INC.
K053099 11/03/2005 BIOHORIZONS PLASTIC TEMPORARY ABUTMENTS BIOHORIZONS IMPLANT SYSTEMS, INC.
K053152 11/10/2005 BIOHORIZONS SINGLE-STAGE IMPLANT BIOHORIZONS IMPLANT SYSTEMS, INC.
K073268 11/20/2007 BIOHORIZONS INTERNAL IMPLANT SYSTEM BIOHORIZONS IMPLANT SYSTEMS, INC.
K073282 11/21/2007 BIOHORIZONS SINGLE-STAGE IMPLANT SYSTEM BIOHORIZONS IMPLANT SYSTEMS, INC.
K032351 07/30/2003 THE MAESTRO SYSTEM 3.0MM DIAMETER IMPLANT BIOHORIZONS IMPLANT SYSTEMS, INC.
K993493 10/15/1999 THE AUTOTAC SYSTEM BIOHORIZONS IMPLANT SYSTEMS, INC.


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