FDA 510(k) Applications Submitted by SHARI L JEFFERS

FDA 510(k) Number	Submission Date	Device Name	Applicant
K980103	01/12/1998	ACUMED SUTURE ANCHOR	ACUMED, INC.
K992525	07/28/1999	ACUMED MODULAR SHOULDER SYSTEM	ACUMED, INC.
K012655	08/13/2001	CONGRUENT BONE PLATE SYSTEM	ACUMED, INC.
K993657	10/28/1999	ACUMED SUTURE ANCHOR	ACUMED, INC.
K013616	11/05/2001	POLARUS CAP SCREW	ACUMED, INC.
K960651	02/15/1996	CERCLAGE WIRE CRIMP BLOCK	ACU-MED, INC.
K960711	02/21/1996	ACUMED BONE GRAFT SYSTEM	ACUMED, INC.
K962091	05/29/1996	POLARUS AF ROD	ACUMED, INC.
K963026	08/05/1996	TBD	ACUMED, INC.
K963077	08/08/1996	TBD	ACUMED, INC.
K963118	08/12/1996	EXTREMITY BONE SCREW	ACUMED, INC.
K954148	09/05/1995	SUTURE WASHER	ACUMED, INC.
K964500	11/08/1996	ACUMED TENSION BAND PIN	ACUMED, INC.
K965028	12/17/1996	ACUMED SUTURE WASHER	ACUMED, INC.
K965029	12/17/1996	STABLELOC II EXTERNAL FIXATOR	ACUMED, INC.