FDA 510(k) Applications Submitted by CAROL E JONES

FDA 510(k) Number Submission Date Device Name Applicant
K020088 01/10/2002 MODIFICATION OF THE BIOPLATE ZIP CRANIOTOMY FIXATION SYSTEM BIOPLATE, INC.
K030806 03/13/2003 BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY BIOPLATE, INC.
K980983 03/17/1998 THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY BIOMEDICS
K031028 04/01/2003 THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY BIOPLATE, INC.
K011380 05/07/2001 MODIFICATION TO THE BIOPLATE BIOCLIP CRANIOTOMY FIXATION SYSTEM BIOPLATE, INC.
K021684 05/22/2002 THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY BIOPLATE, INC.
K972463 07/01/1997 THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY BIOMEDICS
K002426 08/08/2000 THE BIOPLATE REGID FIXATION BONE PLATING SYSTEM FOR CRANOMAXILLOFACIAL SURGERY BIOPLATE, INC.
K022890 08/30/2002 MODIFIED SCREW DESIGNS FOR USE WITH THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY BIOPLATE, INC.
K013050 09/11/2001 THE BIOPLATE ZIP CRANIOTOMY FIXATION SYSTEM BIOPLATE, INC.
K013055 09/11/2001 THE BIOPLATE BIOCLIP CRANIOTOMY FIXATION SYSTEM BIOPLATE, INC.
K023665 10/31/2002 MODIFICATION TO BIOPLATE RIGID BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY BIOPLATE, INC.


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