Bridger Biomed, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Bridger Biomed, Inc. General & Plastic Surgery ✕
4 devices
Cleared
Jan 26, 2001
MODIFICATION TO FLUROTEX SURGICAL MESH
General & Plastic Surgery
38d
Cleared
Jan 26, 2001
MODIFICATION TO FLUOROTEX II SURGICAL MESH
General & Plastic Surgery
38d
Cleared
Aug 26, 2000
FLUOROTEX II SURGICAL MESH
General & Plastic Surgery
24d
Cleared
Jan 07, 1999
FLUOROTEX SURGICAL MESH
General & Plastic Surgery
45d