FDA 510(k) Applications Submitted by MARY-CATHERINE DILLON

FDA 510(k) Number	Submission Date	Device Name	Applicant
K000080	01/11/2000	ASNIS III CANNULATED SCREW SYSTEM	HOWMEDICA OSTEONICS CORP.
K000636	02/25/2000	STRYKER TRAUMA PLATING SYSTEM	HOWMEDICA OSTEONICS CORP.
K001147	04/10/2000	ENHANCED POLYETHYLENE KNEE PROSTHESES	HOWMEDICA OSTEONICS CORP.
K001272	04/20/2000	XIA SPINE SYSTEM	HOWMEDICA OSTEONICS CORP.
K001319	04/26/2000	XIA SPINE SYSTEM HOOKS	HOWMEDICA OSTEONICS CORP.
K001614	05/25/2000	STRYKER TRAUMA PELVIC SET	HOWMEDICA OSTEONICS CORP.
K011643	05/29/2001	SCORPIO CR SUPERFLEX TIBIAL INSERT	HOWMEDICA OSTEONICS CORP.
K001653	05/30/2000	XIA SPINE SYSTEM SACRAL BLOCK ASSEMBLY	HOWMEDICA OSTEONICS CORP.
K001844	06/19/2000	MODIFICATION TO CENTAUR SPINAL SYSTEM	HOWMEDICA OSTEONICS CORP.
K012172	07/12/2001	DURACON PS LIPPED TIBIAL INSERT	HOWMEDICA OSTEONICS
K002505	08/15/2000	XIA SPINE SYSTEM	HOWMEDICA OSTEONICS CORP.
K002858	09/13/2000	XIA SPINE SYSTEM	HOWMEDICA OSTEONICS CORP.
K993077	09/14/1999	HOWMEDICA OSTEONICS RESTORATION HA HIP STEM	HOWMEDICA OSTEONICS CORP.
K993181	09/23/1999	HOWMEDICA OSTEONICS ACCP SYSTEM CORTICAL SCREWS	HOWMEDICA OSTEONICS CORP.
K993402	10/08/1999	OPUS SPINAL SYSTEM	HOWMEDICA OSTEONICS CORP.
K994207	12/14/1999	HOWMEDICA OSTEONICS MODULAR ROTATING HINGE KNEE	HOWMEDICA OSTEONICS CORP.
K994347	12/23/1999	CENTAUR SPINAL SYSTEM	HOWMEDICA OSTEONICS CORP.