FDA 510(k) Applications Submitted by ERIC V HOHENSTEIN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K001530	05/17/2000	THE BIOPLATE BIOCLIP CRANIOTOMY FIXATION SYSTEM	BIOPLATE, INC.
K992330	07/12/1999	THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY	BIOMEDICS
K052297	08/23/2005	POREX ELECTROSURGERY NEEDLE	POREX SURGICAL, INC.
K012908	08/30/2001	BIOPLATE RESORBABLE BONE SCREW	BIOPLATE, INC.
K002879	09/15/2000	MODIFICATION TO BIOPLATE BIOCLIP CRANIOTOMY FIXATION SYSTEM	BIOPLATE, INC.
K994060	11/30/1999	THE BIOPLATE RESORBABLE BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY, BIOLACTATE	BIOPLATE, INC.
K984583	12/24/1998	THE BIOPLATE SHUNT CONNECTOR	BIOMEDICS