FDA 510(k) Applications Submitted by DANNY HODGEMAN

FDA 510(k) Number Submission Date Device Name Applicant
K980102 01/12/1998 BTI HUMERAL INTRAMEDULLARY ROD SYSTEM BIODYNAMIC TECHNOLOGIES, INC.
K990436 02/11/1999 ULTIMAX TROCHANTERIC INTRAMEDULLARY ROD SYSTEM BIODYNAMIC TECHNOLOGIES, INC.
K990481 02/16/1999 ULTIMAX DISTAL RADIAL (VOLAR) LOCKING PLATE SYSTEM BIODYNAMIC TECHNOLOGIES, INC.
K990513 02/18/1999 ULTIMAX CORTICAL BONE SCREWS BIODYNAMIC TECHNOLOGIES, INC.
K970897 03/11/1997 BTI DISTAL FEMORAL INTRAMEDULLARY ROD SYSTEM BIODYNAMIC TECHNOLOGIES, INC.
K981230 04/03/1998 ULTIMAX DISTAL FEMORAL INTRAMEDULLARY ROD SYSTEM BIODYNAMIC TECHNOLOGIES, INC.
K972403 06/26/1997 BTI CORTICAL BONE SCREWS BIODYNAMIC TECHNOLOGIES, INC.
K962552 07/01/1996 EZ-6 PROXIMAL HUMERAL INTERAMEDULLARY ROD SYSTEM BIODYNAMIC TECHNOLOGIES, INC.
K962553 07/01/1996 EZ-FIX MIDSHAFT HUMERAL INTRAMEDULLARY ROD SYSTEM BIODYNAMIC TECHNOLOGIES, INC.
K962706 07/12/1996 EZ-FIX CANNULATED SCREW SYSTEM BIODYNAMIC TECHNOLOGIES, INC.
K962846 07/22/1996 EZ-FIX COMPRESSION HIP/SUPRACONDYLAR SCREW (CHS) SYSTEM BIODYNAMIC TECHNOLOGIES, INC.
K962987 08/01/1996 EZ-FIX SMALL CANNULATED SCREW SYSTEM BIODYNAMIC TECHNOLOGIES, INC.
K974756 12/19/1997 BTI LARGE (7.0MM) CANNULATED TRANSFIXING SCREWS BIODYNAMIC TECHNOLOGIES, INC.


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