Device Classification Name |
Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene
More FDA Info for this Device |
510(K) Number |
K973178 |
Device Name |
Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene |
Applicant |
BRIDGER BIOMED, INC.
2430 NORTH 7TH AVE., SUITE 4
BOZEMAN, MT 59715 US
Other 510(k) Applications for this Company
|
Contact |
BRUCE G RUEFER
Other 510(k) Applications for this Contact |
Regulation Number |
870.3470
More FDA Info for this Regulation Number |
Classification Product Code |
DXZ
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
08/25/1997 |
Decision Date |
11/24/1997 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
CV - Cardiovascular |
Review Advisory Committee |
CV - Cardiovascular |
Statement / Summary / Purged Status |
Summary |
Type |
Traditional |
Reviewed By Third Party |
N |
Expedited Review |
|