FDA 510(k) Applications Submitted by BRUCE G RUEFER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K980548	02/12/1998	DURA-PATCH MODEL DP-XXX	BRIDGER BIOMED, INC.
K002351	08/02/2000	FLUOROTEX II SURGICAL MESH	BRIDGER BIOMED, INC.
K973178	08/25/1997	FLUORO-TEX SURGICAL MEMBRANE	BRIDGER BIOMED, INC.
K964656	11/20/1996	TEFGEN GUIDED TISSUE MEMBRANE	AMERICAN CUSTOM MEDICAL, INC.
K984197	11/23/1998	FLUOROTEX SURGICAL MESH	BRIDGER BIOMED, INC.
K994032	11/26/1999	FLUORO-TEX CARDIOVASCULAR PATCH	BRIDGER BIOMED, INC.
K003906	12/19/2000	MODIFICATION TO FLUROTEX SURGICAL MESH	BRIDGER BIOMED, INC.
K003917	12/19/2000	MODIFICATION TO FLUOROTEX II SURGICAL MESH	BRIDGER BIOMED, INC.
K965205	12/26/1996	TEFGEN - LS	AMERICAN CUSTOM MEDICAL, INC.