Medical Device Manufacturer · US , Bozeman , MT

Bridger Biomed, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1997

Recent clearances: MODIFICATION TO FLUROTEX SURGICAL MESH, MODIFICATION TO FLUOROTEX II SURGICAL MESH, FLUOROTEX II SURGICAL MESH

View 7 510(k) Devices ↓

7

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Bridger Biomed, Inc. Neurology ✕

1 devices

1-1 of 1

Cleared May 13, 1998

DURA-PATCH MODEL DP-XXX

Neurology · 90d