Bridger Biomed, Inc. - FDA 510(k) Cleared Devices
Recent clearances: FLUOROTEX SURGICAL MESH, DURA-PATCH MODEL DP-XXX, FLUORO-TEX SURGICAL MEMBRANE
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Bridger Biomed, Inc. Cardiovascular ✕
2 devices