FDA 510(k) Applications Submitted by BRIDGER BIOMED, INC.

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.
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.


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