Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K070938
Device Classification Name
More FDA Info for this Device
510(K) Number
K070938
Device Name
THROMBI-PASTE THROMBIN/GELATIN POWDER PASTE HEMOSTAT
Applicant
VASCULAR SOLUTIONS, INC.
6464 SYCAMORE COURT
MINNEAPOLIS, MN 55369 US
Other 510(k) Applications for this Company
Contact
JAMES CHAPMAN
Other 510(k) Applications for this Contact
Regulation Number
More FDA Info for this Regulation Number
Classification Product Code
QSX
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/04/2007
Decision Date
08/06/2007
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
-
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact