FDA 510(k) Applications Submitted by MITEK WORLDWIDE

FDA 510(k) Number	Submission Date	Device Name	Applicant
K032167	07/16/2003	BIO-INTRAFIX TIBIAL SCREW AND SHEATH	MITEK WORLDWIDE
K032717	09/02/2003	BIOCRYL RAPIDE INTERFERENCE SCREW	MITEK WORLDWIDE
K021953	06/13/2002	MITEK PDS/PGA STAPLE	MITEK WORLDWIDE
K023388	10/09/2002	MITEK RAPIDLOC-PDS MENISCAL REPAIR SYSTEM	MITEK WORLDWIDE
K030995	03/31/2003	MINILOK QUICKANCHOR PLUS	MITEK WORLDWIDE
K031519	05/15/2003	CUFFLOK ANCHOR	MITEK WORLDWIDE
K021883	06/07/2002	BIOFASTIN RC THREADED SUTURE ANCHOR	MITEK WORLDWIDE
K024115	12/13/2002	MICROFIX QUICKANCHOR PLUS	MITEK WORLDWIDE
K031406	05/05/2003	EXOJET TISSUE MANAGEMENT SYSTEM	MITEK WORLDWIDE
K032078	07/07/2003	MITEK MICRO QUICKANCHOR	MITEK WORLDWIDE