Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K071246
Device Classification Name
Device, Neurovascular Embolization
More FDA Info for this Device
510(K) Number
K071246
Device Name
Device, Neurovascular Embolization
Applicant
MICRUS ENDOVASCULAR CORPORATION
821 FOX LANE
SAN JOSE, CA 95131 US
Other 510(k) Applications for this Company
Contact
PATRICK LEE
Other 510(k) Applications for this Contact
Regulation Number
882.5950
More FDA Info for this Regulation Number
Classification Product Code
HCG
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
05/03/2007
Decision Date
06/01/2007
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact