FDA 510(k) Applications Submitted by THOMAS M MAGUIRE

FDA 510(k) Number	Submission Date	Device Name	Applicant
K010121	01/16/2001	STERILE BUTTON PLATE	SYNTHES (USA)
K010321	02/02/2001	MODULAR FOOT SYSTEM - 2.7 MM MODULE	SYNTHES (USA)
K010499	02/21/2001	SYNTHES (USA) MIDFACE DISTRACTOR	SYNTHES (USA)
K010518	02/22/2001	SYNTHES ANTEROLATERAL CALCANEAL PLATE	SYNTHES (USA)
K010527	02/22/2001	SYNTHES (USA) IMF SCREWS	SYNTHES (USA)
K010690	03/08/2001	SYNTHES TITANIUM MULTI-VECTOR DISTRACTOR	SYNTHES (USA)
K011170	04/17/2001	SYNTHES 2.7 MM LC-DCP, 3.5 MM PROFILE	SYNTHES (USA)
K011583	05/23/2001	SPIKED WASHER	SYNTHES (USA)
K002271	07/26/2000	2.4MM CORTEX SCREW, SELF-TAPPING	SYNTHES (USA)
K012589	08/10/2001	FAST SET PUTTY	SYNTHES (USA)
K002729	09/01/2000	SYNTHES PROXIMAL HUMERAL NAIL	SYNTHES (USA)
K002935	09/21/2000	SYNTHES 1.5MM TI BROW LIFT SCREW	SYNTHES (USA)
K003393	11/01/2000	MAXILLARY DISTRACTOR	SYNTHES (USA)
K003527	11/16/2000	MODIFICATION TO SYNTHES (USA) POLYPIN	SYNTHES (USA)
K003700	12/01/2000	SYNTHES HAMSTRING LOOP	SYNTHES (USA)
K003786	12/08/2000	SMF RESORBABLE MESHES AND SHEETS	SYNTHES (USA)
K003788	12/08/2000	SYNTHES RESORABLE MESHES AND SHEETS	SYNTHES (USA)